Allele Registry

Canonical Allele Identifier: PA645497050

Gene: WWOX HGNC NCBI

ClinVar RCV:

RCV000493095

RCV001080385

ClinVar Variation:

410088

HGVS (amino-acid)	Matching Registered Transcripts
NP_057457.1:p.Ala141Thr	CA8183213 NM_016373.4:c.421G>A