Allele Registry

Canonical Allele Identifier: PA2826464437

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000567489

RCV000662462

RCV001039308

RCV003153734

RCV004000846

ClinVar Variation:

479787

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Arg468Leu	CA029754 NM_001258281.1:c.1403G>T