Canonical Allele Identifier: PA658815269
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 540232
ClinVar RCV Id: RCV000650201
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057457.1:p.Thr358Ile
CA396536963
NM_016373.4:c.1073C>T