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ncbi-variation

by pipeworx-io

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    • F
      license
      Not graded
      quality
      C
      maintenance
      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.
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    • A
      license
      B
      quality
      D
      maintenance
      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.
      12
      6
      Apache 2.0
    • F
      license
      Not graded
      quality
      Not graded
      maintenance
      An MCP plugin that provides access to NCBI's dbSNP database, allowing developers to retrieve genetic variant information, search for SNPs, and access clinical significance data directly in their development environment.
      1
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