Canonical Allele Identifier: PA2826613652
Gene: FBXL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1921126

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265645.1:p.Thr12Ser
CA365092241
NM_001278716.2:c.35C>G
CA365092243
NM_001278716.2:c.34A>T