Allele Registry

Canonical Allele Identifier: PA916058935

Gene: WWOX HGNC NCBI

ClinVar RCV:

RCV000551267

RCV003153725

ClinVar Variation:

473026

HGVS (amino-acid)	Matching Registered Transcripts
NP_570607.1:p.Glu17Asp	CA284502472 NM_130791.4:c.51G>T CA396841831 NM_130791.4:c.51G>C