Allele Registry

Canonical Allele Identifier: PA2826465279

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV003182931

ClinVar Variation:

2453476

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Glu665Lys	CA346729404 NM_001258281.1:c.1993G>A