Allele Registry

Canonical Allele Identifier: PA168573

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000131668

RCV000203979

RCV000410421

RCV000482522

RCV001357874

RCV003150951

ClinVar Variation:

142516

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Gly322Val	CA022651 NM_000251.3:c.965G>T