Canonical Allele Identifier: PA2828136018
Gene: OXCT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 8167
ClinVar RCV Id: RCV000008645
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351229.1:p.Gly226Glu
CA119341
NM_001364300.2:c.677G>A