Allele Registry

Canonical Allele Identifier: PA2826465582

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV001192012

ClinVar Variation:

928239

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Thr746Pro	CA346730267 NM_001258281.1:c.2236A>C