Allele Registry

Canonical Allele Identifier: PA2826465955

Gene: MSH2 HGNC NCBI

ClinVar Allele:

181995

ClinVar RCV:

RCV000167178

RCV000706985

RCV001356340

RCV003995570

ClinVar Variation:

187449

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Ile840Arg	CA020901 NM_001258281.1:c.2519T>G