Allele Registry

Canonical Allele Identifier: PA658672391

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000532242

RCV000562767

RCV004003732

ClinVar Variation:

455485

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Thr456Ile	CA028117 NM_000251.3:c.1367C>T