Allele Registry

Canonical Allele Identifier: PA2826464516

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000076214

RCV000491028

RCV000985797

RCV003452846

RCV003593895

ClinVar Variation:

90717

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Ser488Gly	CA018814 NM_001258281.1:c.1462A>G