Canonical Allele Identifier: PA2580528344
Gene: FBXO39 HGNC NCBI

Linked Data

ClinVar Variation Id: 2370970
ClinVar RCV Id: RCV004207759
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_694962.1:p.Thr328Ile
CA8332527
NM_153230.3:c.983C>T