Canonical Allele Identifier: PA109038
Gene: OXCT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 8166
ClinVar RCV Id: RCV000008644 RCV001091907
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000427.1:p.Gly324Glu
CA119340
NM_000436.4:c.971G>A