Allele Registry

Canonical Allele Identifier: PA2826464704

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000556013

RCV000570637

RCV000588090

RCV003470712

ClinVar Variation:

455526

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Val532Met	CA031369 NM_001258281.1:c.1594G>A