Canonical Allele Identifier: PA2826816326
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 946158
ClinVar RCV Id: RCV001216959 RCV003259162
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278926.1:p.Cys269Tyr
CA8183760
NM_001291997.2:c.806G>A