Canonical Allele Identifier: PA2826613974
Gene: FBXL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 224911

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265645.1:p.Leu481Pro
CA3933439
NM_001278716.2:c.1442T>C