Canonical Allele Identifier: PA916070716
Gene: FBXO38 HGNC NCBI

Linked Data

ClinVar Variation Id: 541003
ClinVar RCV Id: RCV001027484 RCV002235508 RCV002499116 RCV003432699 RCV003937973 RCV004025822
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_995308.1:p.Leu311Ile
CA3497149
NM_205836.3:c.931C>A