Canonical Allele Identifier: PA2828136292
Gene: OXCT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 8164
ClinVar RCV Id: RCV000008642

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351232.1:p.Cys270Phe
CA119339
NM_001364303.2:c.809G>T