Allele Registry

Canonical Allele Identifier: PA658736610

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000580126

ClinVar Variation:

489948

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Cys199Gly	CA346731038 NM_000251.3:c.595T>G