Canonical Allele Identifier: PA2826816319
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 235284
ClinVar RCV Id: RCV000224270 RCV000437104 RCV001081219 RCV002243897 RCV002243898
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278926.1:p.Arg268Cys
CA8183758
NM_001291997.2:c.802C>T