Canonical Allele Identifier: PA2826614045
Gene: FBXL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 437810
ClinVar RCV Id: RCV000499670

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265645.1:p.Leu587Pro
CA3933347
NM_001278716.2:c.1760T>C