Canonical Allele Identifier: PA916018409
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 410086
ClinVar RCV Id: RCV000458450 RCV000764078 RCV001537501
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278926.1:p.Arg75Ser
CA8183335
NM_001291997.2:c.223C>A