Allele Registry

Canonical Allele Identifier: PA2826465035

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000076362

RCV001723648

RCV003452881

ClinVar Variation:

90860

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Gly608Arg	CA019825 NM_001258281.1:c.1822G>C