Allele Registry

Canonical Allele Identifier: PA645472020

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000234549

RCV000519279

RCV000766744

RCV001026663

RCV003998765

ClinVar Variation:

237406

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Ser255Asn	CA040340 NM_000251.3:c.764G>A