Canonical Allele Identifier: PA113699
Gene: FBXL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 66092
ClinVar RCV Id: RCV000056329
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265645.1:p.Gly568Ala
CA144889
NM_001278716.2:c.1703G>C