Canonical Allele Identifier: PA2830313024
Gene: FBXO39 HGNC NCBI

Linked Data

ClinVar Variation Id: 3093709
ClinVar RCV Id: RCV004388992

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_694962.1:p.His264Arg
CA397762311
NM_153230.3:c.791A>G