Allele Registry

Canonical Allele Identifier: PA645475573

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000215978

RCV001222233

RCV003454615

ClinVar Variation:

229891

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Asp758Tyr	CA10578001 NM_000251.3:c.2272G>T