Allele Registry

Canonical Allele Identifier: PA2826464661

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000562329

RCV000696814

RCV004000863

ClinVar Variation:

479851

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Glu524Asp	CA031214 NM_001258281.1:c.1572A>C CA346728270 NM_001258281.1:c.1572A>T