Canonical Allele Identifier: PA2829864980
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1315658
ClinVar RCV Id: RCV001755320

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057457.1:p.Asp10Tyr
CA396841775
NM_016373.4:c.28G>T