Canonical Allele Identifier: PA916058933
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 569653

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570607.1:p.Thr12Arg
CA396841793
NM_130791.4:c.35C>G