Allele Registry

Canonical Allele Identifier: PA357420

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000204459

RCV000480096

RCV000772140

RCV003997653

ClinVar Variation:

220812

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Lys197Glu	CA348678 NM_000251.3:c.589A>G