Canonical Allele Identifier: PA2828136067
Gene: OXCT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 242800
ClinVar RCV Id: RCV000530890 RCV000676890 RCV003907905
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351230.1:p.Thr58Met
CA031340
NM_001364301.2:c.173C>T