Canonical Allele Identifier: PA2826816135
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 571389
ClinVar RCV Id: RCV000692524

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278926.1:p.Asp163Glu
CA8183505
NM_001291997.2:c.489C>G
CA396843102
NM_001291997.2:c.489C>A