Allele Registry

Canonical Allele Identifier: PA331592

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000821319

RCV001022532

RCV001358250

RCV003452941

ClinVar Variation:

91099

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Gly149Asp	CA021170 NM_000251.3:c.446G>A