Canonical Allele Identifier: PA2829864989
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 2313577
ClinVar RCV Id: RCV002892724

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057457.1:p.Pro20Ser
CA8182983
NM_016373.4:c.58C>T