Canonical Allele Identifier: PA2826614032
Gene: FBXL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 437798
ClinVar RCV Id: RCV000504325
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265645.1:p.Pro574Gln
CA3933359
NM_001278716.2:c.1721C>A