Allele Registry

Canonical Allele Identifier: PA2826465759

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000462770

RCV000491706

RCV001356868

ClinVar Variation:

408540

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Gly792Arg	CA036678 NM_001258281.1:c.2374G>A CA346730956 NM_001258281.1:c.2374G>C