Ncbi Variation
Server Details
dbSNP refSNP records and HGVS/SPDI/rsID normalization for human genetic variants, from NCBI…
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- Status
- Unhealthy
- Last Tested
- Transport
- Streamable HTTP
- URL
- Repository
- pipeworx-io/mcp-ncbi-variation
- GitHub Stars
- 0
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- FlicenseNot gradedqualityCmaintenanceEnables resolving genetic variant identifiers (HGVS, dbSNP, ClinVar, gnomAD) to stable ClinGen Allele Registry IDs (CA#) and cross-references, providing a canonical allele identity across genome builds.-
- AlicenseAqualityAmaintenanceGrounds gene-nomenclature work in the HUGO Gene Nomenclature Committee (HGNC) dataset, enabling resolution of gene symbols and IDs to canonical HGNC identifiers, plus cross-references and batch operations.9MIT
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