Allele Registry

Canonical Allele Identifier: PA2826465228

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000508020

RCV000776722

RCV001539955

RCV002527341

RCV004003548

ClinVar Variation:

439190

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Gln652Glu	CA346729326 NM_001258281.1:c.1954C>G