Allele Registry

Canonical Allele Identifier: PA168121

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000131412

RCV000411200

RCV000479306

RCV000524419

RCV000781566

RCV001357533

ClinVar Variation:

91189

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Arg243Gln	CA022108 NM_000251.3:c.728G>A