Canonical Allele Identifier: PA916066040
Gene: FBXL8 HGNC NCBI

Linked Data

ClinVar Variation Id: 320168
ClinVar RCV Id: RCV000357401

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060848.2:p.Glu364Lys
CA8101613
NM_018378.3:c.1090G>A