Canonical Allele Identifier: PA645497050
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 410088
ClinVar RCV Id: RCV000493095 RCV001080385
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057457.1:p.Ala141Thr
CA8183213
NM_016373.4:c.421G>A