Canonical Allele Identifier: PA2826613737
Gene: FBXL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 437576
ClinVar RCV Id: RCV000502106
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265645.1:p.Val140Ile
CA3933691
NM_001278716.2:c.418G>A