Allele Registry

Canonical Allele Identifier: PA160879

Gene: MSH2 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score -3.6863640255

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000034556

RCV000121564

RCV000129519

RCV001030484

RCV001080801

RCV001093691

RCV001356651

RCV001787035

RCV004534720

ClinVar Variation:

41648

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Glu809Lys	CA020577 NM_000251.3:c.2425G>A