Canonical Allele Identifier: PA2826537465
Gene: FBXO38 HGNC NCBI

Linked Data

ClinVar Variation Id: 2756418
ClinVar RCV Id: RCV003597033

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258652.1:p.Glu83Lys
CA361654305
NM_001271723.2:c.247G>A