Canonical Allele Identifier: PA2829864994
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1474088
ClinVar RCV Id: RCV001969693

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057457.1:p.Trp22Cys
CA396841857
NM_016373.4:c.66G>T
CA396841858
NM_016373.4:c.66G>C