Allele Registry

Canonical Allele Identifier: PA916018397

Gene: WWOX HGNC NCBI

ClinVar RCV:

RCV000493095

RCV001080385

ClinVar Variation:

410088

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278926.1:p.Ala28Thr	CA8183213 NM_001291997.2:c.82G>A