Canonical Allele Identifier: PA2828136240
Gene: OXCT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 8164
ClinVar RCV Id: RCV000008642
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351231.1:p.Cys426Phe
CA119339
NM_001364302.2:c.1277G>T