Canonical Allele Identifier: PA2828136122
Gene: OXCT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 8166

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351230.1:p.Gly322Glu
CA119340
NM_001364301.2:c.965G>A