Allele Registry

Canonical Allele Identifier: PA2826463607

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000076778

RCV000160579

RCV000216069

RCV000630153

RCV001535593

RCV002281913

ClinVar Variation:

91273

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Cys267Tyr	CA022722 NM_001258281.1:c.800G>A