Canonical Allele Identifier: PA891852175
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 569654
ClinVar RCV Id: RCV000690342
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057457.1:p.Leu18Met
CA396841832
NM_016373.4:c.52C>A