Canonical Allele Identifier: PA2826614004
Gene: FBXL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 437776
ClinVar RCV Id: RCV000500384
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265645.1:p.Gln531Arg
CA3933417
NM_001278716.2:c.1592A>G