Canonical Allele Identifier: PA109018
Gene: OXCT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 8164
ClinVar RCV Id: RCV000008642
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000427.1:p.Cys456Phe
CA119339
NM_000436.4:c.1367G>T