Canonical Allele Identifier: PA916058928
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 656357
ClinVar RCV Id: RCV000812755
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570607.1:p.Ala3Val
CA396841741
NM_130791.4:c.8C>T