Allele Registry

Canonical Allele Identifier: PA645509907

Gene: MSH2 HGNC NCBI

MaveDb:

Score -3.1828115509

ClinVar RCV:

RCV000507809

RCV000541857

RCV000572189

RCV000986669

RCV004003546

ClinVar Variation:

439186

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Arg444His	CA346724650 NM_000251.3:c.1331G>A