Canonical Allele Identifier: PA2826537728
Gene: FBXO38 HGNC NCBI

Linked Data

ClinVar Variation Id: 541019
ClinVar RCV Id: RCV002235515

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258652.1:p.Asp597Glu
CA361655435
NM_001271723.2:c.1791T>A
CA361655437
NM_001271723.2:c.1791T>G