Allele Registry

Canonical Allele Identifier: PA2826626474

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000160673

RCV000212653

RCV000304378

RCV000410091

RCV000524120

RCV001193697

RCV001798554

ClinVar Variation:

182628

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Cys485Ser	CA009314 NM_001281492.2:c.1454G>C CA346749634 NM_001281492.2:c.1453T>A