Canonical Allele Identifier: PA916018407
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 473027
ClinVar RCV Id: RCV000524996 RCV001726237 RCV002483483
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278926.1:p.Ala66Ser
CA8183322
NM_001291997.2:c.196G>T