Allele Registry

Canonical Allele Identifier: PA2826463558

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000131668

RCV000203979

RCV000410421

RCV000482522

RCV001357874

RCV003150951

ClinVar Variation:

142516

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Gly256Val	CA022651 NM_001258281.1:c.767G>T