Allele Registry

Canonical Allele Identifier: PA2826627547

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000222631

RCV000479488

RCV000524146

RCV000662498

RCV000759136

RCV003137607

RCV003997079

RCV004542741

ClinVar Variation:

89291

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Lys736Thr	CA010469 NM_001281492.2:c.2207A>C