Allele Registry

Canonical Allele Identifier: PA2826627924

Gene: MSH6 HGNC NCBI

Linked Data

ClinVar RCV:

RCV000213285

RCV000485366

RCV000555735

RCV000781579

RCV001355880

RCV003335237

RCV003462414

RCV003997779

ClinVar Variation:

229879

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Glu823Lys	CA069715 NM_001281492.2:c.2467G>A