Canonical Allele Identifier: PA2826816289
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1047640
ClinVar RCV Id: RCV001352381
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278926.1:p.Cys249Arg
CA396536991
NM_001291997.2:c.745T>C