Allele Registry

Canonical Allele Identifier: PA645475937

Gene: MSH2 HGNC NCBI

MaveDb:

Score -4.4840087877

ClinVar RCV:

RCV000462770

RCV000491706

RCV001356868

ClinVar Variation:

408540

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Gly858Arg	CA036678 NM_000251.3:c.2572G>A CA346730956 NM_000251.3:c.2572G>C