Canonical Allele Identifier: PA916058993
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 383820
ClinVar RCV Id: RCV000544935 RCV001291668 RCV001697771
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570607.1:p.Thr111Ser
CA8183162
NM_130791.4:c.332C>G
CA396842482
NM_130791.4:c.331A>T