Canonical Allele Identifier: PA113672
Gene: FBXL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 66093

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265645.1:p.Arg482Trp
CA144891
NM_001278716.2:c.1444C>T