Canonical Allele Identifier: PA2829865003
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1057897
ClinVar RCV Id: RCV001366966
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057457.1:p.Val32Ile
CA396841924
NM_016373.4:c.94G>A