Canonical Allele Identifier: PA2828136226
Gene: OXCT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 8166

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351231.1:p.Gly324Glu
CA119340
NM_001364302.2:c.971G>A