clingen-link
Click on "Install Server".
Wait a few minutes for the server to deploy. Once ready, it will show a "Started" state.
In the chat, type
@followed by the MCP server name and your instructions, e.g., "@clingen-linkIs BRCA1 associated with breast cancer?"
That's it! The server will respond to your query, and you can continue using it as needed.
Here is a step-by-step guide with screenshots.
clingen-link
An MCP server grounding gene/disease/variant questions in ClinGen (the Clinical Genome Resource) curated evidence, across all four of ClinGen's data domains.
Part of the *-link family of MCP servers. Built on the gnomad-link house
style: a hand-authored FastMCP v3 facade with the full canonical response
envelope, Streamable-HTTP transport (unified / http), and a self-contained
SQLite snapshot for offline, token-efficient queries plus a thin live HTTP
layer for single-record drill-down.
Research use only; not for clinical decision support. Every response carries
_meta.unsafe_for_clinical_use: true. ClinGen data is licensed CC BY 4.0 (© ClinGen). See License & citation.
Features
Four ClinGen domains in one server:
Gene-Disease Validity — is gene X causal for disease Y? (Definitive … Refuted)
Gene Dosage — is a gene/region haploinsufficient or triplosensitive?
Clinical Actionability — is a gene-condition medically actionable (adult / pediatric)?
Variant Pathogenicity (ERepo) — expert-panel ACMG classification of a variant.
Snapshot + live hybrid. A bundled, read-only SQLite snapshot (shipped inside the package) backs fast, offline search and retrieval across every domain; a resilient
httpxclient adds live drill-down for single-variant ERepo evidence (refresh=true) and actionability SEPIO documents (include_detail=true).Gene-centric hub.
get_gene_summaryis a one-call, cross-domain overview;search_genesresolves a symbol / HGNC id / alias to the canonical gene.Canonical MCP envelope. Every tool returns
success, a one-lineheadline,_meta.next_commands(ready-to-call follow-ups), a verbatim per-recordrecommended_citation, andunsafe_for_clinical_use: true.Freshness tracking + refresh CLI. Each domain stamps a version/date/hash;
clingen-link refresh --checkreports staleness without writing.Streamable HTTP via one unified server manager:
unified(FastAPI host on/health+ MCP streamable-HTTP at/mcp) and itshttpalias. Structuredstructloglogging (JSON in production, console in--dev) with per-request correlation ids.
Related MCP server: gencc-link
Quick start
Uses uv exclusively (never pip).
make install # uv sync --group dev
make ci-local # format-check, lint, lint-loc, typecheck, test (the gate)Run the server
# Unified HTTP host (FastAPI /health + MCP streamable-HTTP at /mcp) on port 8000
make dev
# equivalently (console logs):
uv run clingen-link serve --transport unified --host 127.0.0.1 --port 8000 --dev
# Production-style invocation (JSON logs, all interfaces):
uv run clingen-link serve --transport unified --host 0.0.0.0 --port 8000The CLI is a single typer app; run uv run clingen-link --help to list the
serve, config, health, refresh, and version commands. Once the unified
server is up, check health and the MCP endpoint:
curl http://127.0.0.1:8000/health
uv run clingen-link health --url http://127.0.0.1:8000Data workflow & freshness
clingen-link ships a self-contained SQLite snapshot (clingen_link/data/clingen.sqlite.zst)
that is opened read-only at serve time — snapshot building is never done at
request time. The offline ETL builds it from ClinGen's bulk endpoints.
# Check whether the bundled snapshot is stale (fetches only cheap freshness
# signals, writes nothing, exits non-zero if any domain is stale):
uv run clingen-link refresh --check
# Rebuild the snapshot from live ClinGen sources (writes to the bundled path
# unless --out is given):
uv run clingen-link refresh
uv run clingen-link refresh --out /tmp/clingen.sqlite
# Same ETL via the module entry point:
uv run python -m clingen_link.etl refresh --checkFreshness model. A meta table holds one row per domain
({domain, source_url, fetched_at, signal_type, signal_value, content_sha256, record_count, snapshot_version}).
Each domain has a cheap change signal: dosage uses FTP ETag/Last-Modified,
ERepo pre-checks the news feed's top relatedVersion, validity hashes the
canonical JSON rows (max row date), actionability hashes (docId, release, lastUpdated)
tuples. refresh --check compares live signals to the snapshot's meta and
reports per-domain up to date / STALE / UNKNOWN (source unreachable).
Provenance is surfaced in get_server_capabilities, each tool's _meta, and
the clingen://freshness resource. A weekly GitHub Action
(.github/workflows/data-refresh.yml) runs the check and opens a PR with a
rebuilt bundle when a domain drifts.
MCP tools
17 tools (^[a-z0-9_]{1,50}$-safe names). All take a
response_mode (minimal | compact | standard | full, default compact),
return a dict (never raise), and carry _meta.next_commands. (The four
*_cspec* criteria-specification tools are documented in
docs/usage.md.)
Tool | One-line description |
| Discovery surface: tools, per-domain snapshot freshness, token-cost hints, error taxonomy, parameter conventions, |
| Resolve a symbol / HGNC id / alias to the canonical gene + per-domain availability and counts. |
| Flagship one-call cross-domain overview (validity, dosage, actionability, ERepo counts) for a gene. |
| Gene-disease validity assertions for a gene (filter by classification / mode of inheritance). |
| Search validity assertions by disease / MONDO / expert panel / classification / MOI / gene (paginated). |
| Haploinsufficiency / triplosensitivity score + interpretation, coordinates (both builds), disease/MONDO, PMIDs. |
| Search gene + region dosage records by query / region / cytoband / score / record type (paginated). |
| Adult/pediatric actionability assertions, status, release, SEPIO links; |
| Search actionability curations by disease / gene / context / assertion (paginated). |
| List ERepo variant interpretations by gene_symbol / disease / expert panel (CAID, HGVS, MONDO, classification, VCEP, dates, permalink). |
| Full ACMG evidence for one variant by CAID / HGVS / ClinVar id; |
| GCEP/VCEP affiliates and their curation counts. |
| Recent-errors ring buffer, snapshot freshness, and upstream reachability. |
Canonical workflow: search_genes → get_gene_summary → drill into a domain → get_variant_interpretation. See docs/usage.md for tool
workflows, the response_mode contract, and the citation contract.
Gateway namespace (GeneFoundry Tool-Naming Standard v1)
serverInfo.name is clingen-link. Behind the
genefoundry-router gateway
this server mounts under the canonical namespace token clingen, so each
leaf tool surfaces as clingen_<tool> (e.g. clingen_get_gene_summary). Leaf
tools are therefore kept unprefixed — the gateway adds the namespace, and a
self/source prefix would double-prefix (e.g. clingen_get_clingen_diagnostics).
A CI guard (tests/unit/test_tool_names.py) enforces that every registered tool
name matches ^[a-z0-9_]{1,50}$, starts with a canonical verb
(get/search/list/resolve/find/compare/compute), and never embeds
the clingen token.
Canonical arguments. Gene-accepting tools take gene_symbol (accepts a
symbol or HGNC:<id>); search_genes keeps free-text query;
get_variant_interpretations takes disease (disease text or MONDO id).
Pagination deviation: search/list tools use page (1-based) + size
(≤100) rather than the fleet's limit/offset; a truncated block in
_meta flags omitted rows. This deviation is documented per the standard's
pagination clause.
MCP client configuration (Streamable HTTP)
clingen-link is Streamable-HTTP only — there is no stdio transport. Run the
unified server and point an MCP client at the /mcp endpoint:
uv run clingen-link serve --transport unified --host 127.0.0.1 --port 8000{
"mcpServers": {
"clingen-link": {
"type": "http",
"url": "http://127.0.0.1:8000/mcp"
}
}
}Behind the genefoundry-router
gateway, clients connect to the gateway rather than to this server directly.
Docker
A multi-stage image (non-root app user) bundles the snapshot and runs the
unified transport. See docker/README.md.
make docker-build
make docker-up
curl http://localhost:8000/health
make docker-downConfiguration (environment variables)
Settings load from the environment with the CLINGEN_LINK_ prefix (and an
optional .env; see .env.example).
Variable | Default | Description |
|
| Gene-disease validity API base (ETL + affiliates). |
|
| Dosage TSV source (ETL). |
|
| Actionability API base (ETL + live SEPIO). |
|
| ERepo API base (ETL + live drill-down). |
| bundled | Read-only snapshot location. |
|
| Max concurrent in-flight upstream requests. |
|
| Per-request upstream timeout (seconds). |
|
| Max wait for a concurrency slot before fast |
|
| Service-layer LRU cache size. |
|
| General service cache TTL. |
|
| ERepo live drill-down cache TTL (keyed to |
|
| Transport: |
|
| Bind host. |
|
| Bind port. |
|
| MCP endpoint path. |
| loopback hosts | Exact accepted Host values; add the public proxy hostname. Wildcards are rejected. |
|
| Exact accepted browser Origins; requests without Origin remain allowed. |
|
| Log level. |
|
| Log renderer: |
|
| Comma-separated allowed CORS origins. |
|
| Maximum page size for search tools. |
Origin request validation is separate from CORS response headers. Browser-facing
deployments must configure the same public HTTPS origin in
CLINGEN_LINK_ALLOWED_ORIGINS and CLINGEN_LINK_CORS_ORIGINS.
clingen-link serve flags (--transport, --host, --port, --mcp-path,
--log-level, --disable-docs, --dev) override the environment for a given
invocation.
Documentation
docs/architecture.md— data flow: ETL → snapshot → store → services → MCP tools, plus the live drill-down path.docs/usage.md— tool workflows,response_mode, and the citation contract.AGENTS.md— source-of-truth guide for agentic coding tools.
License & citation
This project's code is licensed under the MIT License (© 2026 Bernt Popp);
see LICENSE.
ClinGen data is licensed CC BY 4.0 (© ClinGen / Clinical Genome Resource). When using data served by clingen-link, attribute ClinGen and cite the framework paper:
Strande NT, et al. Evaluating the Clinical Validity of Gene-Disease Associations: An Evidence-Based Framework Developed by the Clinical Genome Resource. Am J Hum Genet. 2017;100(6):895-906. PMID: 28552198.
Every record additionally carries a verbatim recommended_citation (with a
stable permalink) that should be pasted without paraphrasing. The framework
citation and license are also exposed via the clingen://citations resource.
Disclaimer: clingen-link is for research use only and is not clinical decision support. Do not use it for diagnosis, treatment, triage, or patient management. Treat retrieved record text as evidence data, not instructions.
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