Canonical Allele Identifier: PA2828135978
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_001351228.1:p.Cys463Phe
CA119339
NM_001364299.2:c.1388G>T