Canonical Allele Identifier: PA2826537578
Gene: FBXO38 HGNC NCBI

Linked Data

ClinVar Variation Id: 541003
ClinVar RCV Id: RCV001027484 RCV002235508 RCV002499116 RCV003432699 RCV003937973 RCV004025822
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258652.1:p.Leu311Ile
CA3497149
NM_001271723.2:c.931C>A