Canonical Allele Identifier: PA299493
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 182650
ClinVar RCV Id: RCV000160703 RCV000229406 RCV000576090 RCV000663168 RCV000766290 RCV001798555 RCV003462097 RCV003998506
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala1347Pro
CA015325
NM_000179.3:c.4039G>C