Allele Registry

Canonical Allele Identifier: PA2826465116

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000490880

RCV000659883

RCV000664310

RCV001209603

ClinVar Variation:

428464

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Gly626Trp	CA346729189 NM_001258281.1:c.1876G>T