Canonical Allele Identifier: PA2829864997
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1039606
ClinVar RCV Id: RCV001343112
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057457.1:p.Thr27del
CA8182985
NM_016373.4:c.80_82del