Allele Registry

Canonical Allele Identifier: PA100029

Gene: WWOX HGNC NCBI

ClinVar RCV:

RCV000087049

ClinVar Variation:

100649

HGVS (amino-acid)	Matching Registered Transcripts
NP_057457.1:p.Pro47Thr	CA150589 NM_016373.4:c.139C>A