Allele Registry

Canonical Allele Identifier: PA330422

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000524133

RCV000568729

RCV000662512

RCV001582560

RCV003466941

RCV003997072

ClinVar Variation:

89259

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Phe726Tyr	CA009822 NM_000179.3:c.2177T>A