Canonical Allele Identifier: PA645497381
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 235284
ClinVar RCV Id: RCV000224270 RCV000437104 RCV001081219 RCV002243897 RCV002243898
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057457.1:p.Arg381Cys
CA8183758
NM_016373.4:c.1141C>T