Canonical Allele Identifier: PA2826613699
Gene: FBXL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 437550
ClinVar RCV Id: RCV000500050
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265645.1:p.Ser67Arg
CA3933721
NM_001278716.2:c.201T>G
CA365090771
NM_001278716.2:c.201T>A
CA365090793
NM_001278716.2:c.199A>C