Canonical Allele Identifier: PA658679959
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 485853
ClinVar RCV Id: RCV000575294 RCV000689038 RCV000985851 RCV001292699
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asn21Asp
CA346734569
NM_000179.3:c.61A>G