Canonical Allele Identifier: PA2828136273
Gene: OXCT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 8166

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351232.1:p.Gly138Glu
CA119340
NM_001364303.2:c.413G>A