Canonical Allele Identifier: PA2826613730
Gene: FBXL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 437568
ClinVar RCV Id: RCV000502661

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265645.1:p.Glu132Lys
CA3933699
NM_001278716.2:c.394G>A