Allele Registry

Canonical Allele Identifier: PA100020

Gene: WWOX HGNC NCBI

ClinVar RCV:

RCV000157088

ClinVar Variation:

180251

HGVS (amino-acid)	Matching Registered Transcripts
NP_057457.1:p.Pro47Arg	CA213108 NM_016373.4:c.140C>G