Canonical Allele Identifier: PA2828135935
Gene: OXCT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 8167
ClinVar RCV Id: RCV000008645

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351228.1:p.Gly226Glu
CA119341
NM_001364299.2:c.677G>A