Allele Registry

Canonical Allele Identifier: PA916058945

Gene: WWOX HGNC NCBI

ClinVar RCV:

RCV000157088

ClinVar Variation:

180251

HGVS (amino-acid)	Matching Registered Transcripts
NP_570607.1:p.Pro47Arg	CA213108 NM_130791.4:c.140C>G