Canonical Allele Identifier: PA2573296802
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1420329
ClinVar RCV Id: RCV001914195
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570607.1:p.Val55Ala
CA8183033
NM_130791.4:c.164T>C