Canonical Allele Identifier: PA2826613998
Gene: FBXL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 437771

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265645.1:p.Thr522Ala
CA3933423
NM_001278716.2:c.1564A>G