Canonical Allele Identifier: PA2826614017
Gene: FBXL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 437785
ClinVar RCV Id: RCV000500747
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265645.1:p.Cys558Gly
CA3933407
NM_001278716.2:c.1672T>G