Allele Registry

Canonical Allele Identifier: PA332431

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000122987

RCV000411448

RCV000563636

RCV002469017

RCV003149838

RCV003997407

ClinVar Variation:

135859

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Lys872Arg	CA020814 NM_000251.3:c.2615A>G