Canonical Allele Identifier: PA2826816313
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 540234
ClinVar RCV Id: RCV000650203 RCV003156275
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278926.1:p.Asn264Lys
CA8183749
NM_001291997.2:c.792C>A
CA396537114
NM_001291997.2:c.792C>G