Canonical Allele Identifier: PA109029
Gene: OXCT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 8167
ClinVar RCV Id: RCV000008645
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000427.1:p.Gly219Glu
CA119341
NM_000436.4:c.656G>A