Canonical Allele Identifier: PA2826613827
Gene: FBXL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 437635
ClinVar RCV Id: RCV000500486 RCV002524374
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265645.1:p.Met259Thr
CA3933617
NM_001278716.2:c.776T>C