Canonical Allele Identifier: PA2829864988
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1037991
ClinVar RCV Id: RCV001341234
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057457.1:p.Leu18Val
CA8182982
NM_016373.4:c.52C>G