Allele Registry

Canonical Allele Identifier: PA2826465255

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000160603

RCV000492028

RCV000629694

RCV003462091

RCV003998478

ClinVar Variation:

182572

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Thr658Met	CA020167 NM_001258281.1:c.1973C>T