Canonical Allele Identifier: PA2826816352
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 567630
ClinVar RCV Id: RCV000687773 RCV002473105
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278926.1:p.Ala281Thr
CA8183779
NM_001291997.2:c.841G>A