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Enables 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.
Copy the install command and let the AI configure it · recommended for beginners
No copy-paste install info for "allele-registry-mcp-server" yet — see the docs or source repo.