Canonical Allele Identifier: PA2826614034
Gene: FBXL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 437802

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265645.1:p.Ala575Ser
CA3933355
NM_001278716.2:c.1723G>T