Allele Registry

Canonical Allele Identifier: PA2826462818

Gene: MSH2 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

96516

ClinVar RCV:

RCV000221964

RCV000412138

RCV000552261

RCV001196697

RCV001353838

RCV003387753

RCV003997169

ClinVar Variation:

91041

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Leu26Val	CA020916 NM_001258281.1:c.76C>G