Allele Registry

Canonical Allele Identifier: PA094760

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000076778

RCV000160579

RCV000216069

RCV000630153

RCV001535593

RCV002281913

ClinVar Variation:

91273

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Cys333Tyr	CA022722 NM_000251.3:c.998G>A