Allele Registry

Canonical Allele Identifier: PA2826465953

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000131745

RCV000235233

RCV000781552

RCV001084144

RCV003997168

ClinVar Variation:

91038

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Thr839Ile	CA020895 NM_001258281.1:c.2516C>T