Allele Registry

Canonical Allele Identifier: PA2826465294

Gene: MSH2 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

171077

ClinVar RCV:

RCV000148638

RCV000411526

RCV000471467

RCV000491584

RCV000588732

RCV001175338

RCV004532667

ClinVar Variation:

161300

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Ile669Val	CA020218 NM_001258281.1:c.2005A>G