Canonical Allele Identifier: PA2828135935
Gene: OXCT1 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

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