Allele Registry

Canonical Allele Identifier: PA645382926

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000213285

RCV000485366

RCV000555735

RCV000781579

RCV001355880

RCV003335237

RCV003462414

RCV003997779

ClinVar Variation:

229879

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Glu953Lys	CA069715 NM_000179.3:c.2857G>A