Canonical Allele Identifier: PA658811789
Gene: FBXO28 HGNC NCBI

Linked Data

ClinVar Variation Id: 521663
ClinVar RCV Id: RCV000624391 RCV001420238 RCV001844206 RCV003311864
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055991.1:p.Arg348Leu
CA344706196
NM_015176.4:c.1043G>T