Allele Registry

Canonical Allele Identifier: PA2826465064

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000160599

RCV000219973

RCV000813805

RCV000814388

RCV002422813

RCV003324799

RCV004001761

ClinVar Variation:

182569

657719

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Gln615His	CA019887 NM_001258281.1:c.1845A>T CA033402 NM_001258281.1:c.1845A>C