Allele Registry

Canonical Allele Identifier: PA330459

Gene: MSH6 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

94765

ClinVar RCV:

RCV000222631

RCV000479488

RCV000524146

RCV000662498

RCV000759136

RCV003137607

RCV003997079

RCV004542741

ClinVar Variation:

89291

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Lys866Thr	CA010469 NM_000179.3:c.2597A>C