Allele Registry

Canonical Allele Identifier: PA100009

Gene: WWOX HGNC NCBI

ClinVar RCV:

RCV000087048

RCV001091765

RCV001891133

ClinVar Variation:

100648

1390703

HGVS (amino-acid)	Matching Registered Transcripts
NP_057457.1:p.Gly372Arg	CA150588 NM_016373.4:c.1114G>C CA396537069 NM_016373.4:c.1114G>A