Canonical Allele Identifier: PA916058935
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 473026

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570607.1:p.Glu17Asp
CA284502472
NM_130791.4:c.51G>T
CA396841831
NM_130791.4:c.51G>C