Canonical Allele Identifier: PA2826614014
Gene: FBXL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1942566
ClinVar RCV Id: RCV002646865

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265645.1:p.Asp552Gly
CA365086439
NM_001278716.2:c.1655A>G