Allele Registry

Canonical Allele Identifier: PA2826464972

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000490598

RCV000491547

RCV001039917

ClinVar Variation:

427603

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Asp594Gly	CA346728864 NM_001258281.1:c.1781A>G