Canonical Allele Identifier: PA891852217
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 571389
ClinVar RCV Id: RCV000692524

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057457.1:p.Asp276Glu
CA8183505
NM_016373.4:c.828C>G
CA396843102
NM_016373.4:c.828C>A