Canonical Allele Identifier: PA2829865012
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1003587
ClinVar RCV Id: RCV001300161
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057457.1:p.Glu40del
CA623605159
NM_016373.4:c.118_120del