Canonical Allele Identifier: PA2829864971
Gene: WWOX HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057457.1:p.Ala3Val
CA396841741
NM_016373.4:c.8C>T