Canonical Allele Identifier: PA2826613982
Gene: FBXL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 437762
ClinVar RCV Id: RCV000504224 RCV002524387
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265645.1:p.Asn495His
CA3933433
NM_001278716.2:c.1483A>C