Allele Registry

Canonical Allele Identifier: PA2826816301

Gene: WWOX HGNC NCBI

ClinVar RCV:

RCV000087048

RCV001091765

RCV001891133

ClinVar Variation:

100648

1390703

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278926.1:p.Gly259Arg	CA150588 NM_001291997.2:c.775G>C CA396537069 NM_001291997.2:c.775G>A