Canonical Allele Identifier: PA645378339
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 237159
ClinVar RCV Id: RCV000229669 RCV000491394 RCV001354734 RCV001572461 RCV003998719
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala84Val
CA10582035
NM_000179.3:c.251C>T