Canonical Allele Identifier: PA916044711
Gene: OXCT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 8166

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351229.1:p.Gly331Glu
CA119340
NM_001364300.2:c.992G>A