Allele Registry

Canonical Allele Identifier: PA2826463052

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000580126

ClinVar Variation:

489948

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Cys133Gly	CA346731038 NM_001258281.1:c.397T>G