Allele Registry

Canonical Allele Identifier: PA274818

Gene: MSH2 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score -1.9241719266

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000129717

RCV000172810

RCV000235177

RCV000524397

RCV000589745

RCV000760996

RCV001354813

RCV003149751

RCV004528276

ClinVar Variation:

91039

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Leu911Arg	CA020910 NM_000251.3:c.2732T>G