Allele Registry

Canonical Allele Identifier: PA2826463247

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000757471

RCV000775779

RCV001046068

RCV001824799

ClinVar Variation:

420794

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Lys182Arg	CA16617562 NM_001258281.1:c.545A>G