Canonical Allele Identifier: PA2573296794
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1474088
ClinVar RCV Id: RCV001969693

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570607.1:p.Trp22Cys
CA396841857
NM_130791.4:c.66G>T
CA396841858
NM_130791.4:c.66G>C