Canonical Allele Identifier: PA2499296221
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1039606
ClinVar RCV Id: RCV001343112

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570607.1:p.Thr27del
CA8182985
NM_130791.4:c.80_82del