Canonical Allele Identifier: PA2826816346
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1432253
ClinVar RCV Id: RCV001941169
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278926.1:p.Glu279Val
CA396537216
NM_001291997.2:c.836A>T