Canonical Allele Identifier: PA144892
Gene: FBXL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 66093
ClinVar RCV Id: RCV000056330 RCV000162170 RCV000224233 RCV003155062 RCV003242974
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036292.2:p.Arg482Trp
CA144891
NM_012160.5:c.1444C>T