Canonical Allele Identifier: PA916070781
Gene: FBXO38 HGNC NCBI

Linked Data

ClinVar Variation Id: 541019
ClinVar RCV Id: RCV002235515

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_995308.1:p.Asp597Glu
CA361655435
NM_205836.3:c.1791T>A
CA361655437
NM_205836.3:c.1791T>G