Canonical Allele Identifier: PA916018394
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 473024
ClinVar RCV Id: RCV000537303 RCV001330929 RCV001507346
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278926.1:p.Ile23Val
CA8183177
NM_001291997.2:c.67A>G