Enables structured queries and data analysis of cancer genomics information by interfacing with the Clinical Interpretation of Variants in Cancer (CIViC) API. It converts GraphQL responses into queryable SQLite tables for efficient clinical interpretation and natural language interaction.
An MCP server that enables access to clinical evidence from the CIViC database, allowing users to search across variants, diseases, drugs, and phenotypes to support precision oncology research.
Provides interpretable variant effect predictions for 4.2 million ClinVar variants using the EVEE API. Enables searching, comparing, and analyzing genetic variants with AI-generated mechanistic interpretations and disruption profiles.
Provides a programmatic interface to the Genome Aggregation Database (gnomAD) API across versions v2.1.1, v3.1.2, and v4.1.0. It enables users to query gene metadata, variant information, population frequencies, and ClinVar data through a unified schema.
