Canonical Allele Identifier: PA645381229
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 233357
ClinVar RCV Id: RCV000222892 RCV000478131 RCV000629954 RCV003998550
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Val653Met
CA10578088
NM_000179.3:c.1957G>A