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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.
复制安装指令，让 AI 自动完成配置 · 推荐新手
"allele-registry-mcp-server" 暂无可直接复制的安装信息，请查看页面文档或源码仓库。