Allele Registry

Canonical Allele Identifier: PA168665

Gene: MSH2 HGNC NCBI

MaveDb:

Score -4.0871955306

ClinVar RCV:

RCV000131729

RCV000487151

RCV001182806

RCV001202065

ClinVar Variation:

142539

922624

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Met300Ile	CA022513 NM_000251.3:c.900G>A CA346732941 NM_000251.3:c.900G>C CA346732942 NM_000251.3:c.900G>T