Canonical Allele Identifier: PA2826613735
Gene: FBXL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 437574
ClinVar RCV Id: RCV000503707
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265645.1:p.Ala139Gly
CA3933692
NM_001278716.2:c.416C>G