Allele Registry

Canonical Allele Identifier: PA2826463867

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000227304

RCV000566323

RCV000662565

RCV000780444

RCV001589170

RCV003998752

ClinVar Variation:

237359

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Ala325Thr	CA10582008 NM_001258281.1:c.973G>A