Canonical Allele Identifier: PA1139727556
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 955091
ClinVar RCV Id: RCV001227667 RCV001819926
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057457.1:p.Leu307Val
CA8183551
NM_016373.4:c.919C>G