Canonical Allele Identifier: PA1139749638
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 938023
ClinVar RCV Id: RCV001207166 RCV002561245
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570607.1:p.Asn36Asp
CA396841951
NM_130791.4:c.106A>G