Allele Registry

Canonical Allele Identifier: PA2826465828

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000122987

RCV000411448

RCV000563636

RCV002469017

RCV003149838

RCV003997407

ClinVar Variation:

135859

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Lys806Arg	CA020814 NM_001258281.1:c.2417A>G