Canonical Allele Identifier: PA2825087615
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1171277
ClinVar RCV Id: RCV001524238 RCV001872024
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Pro343His
CA346741378
NM_000179.3:c.1028C>A