Allele Registry

Canonical Allele Identifier: PA094936

Gene: MSH2 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score -6.037230966

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000076492

RCV000166332

RCV000486446

RCV000765673

RCV000986690

RCV001085048

RCV001354097

RCV003153356

RCV004525868

ClinVar Variation:

90990

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.His839Arg	CA020662 NM_000251.3:c.2516A>G