Canonical Allele Identifier: PA2826625323
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_001268421.1:p.Pro213His
CA346741378
NM_001281492.2:c.638C>A