Canonical Allele Identifier: PA916058951
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 429263
ClinVar RCV Id: RCV000493734
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570607.1:p.Asp58Asn
CA396842111
NM_130791.4:c.172G>A