Canonical Allele Identifier: PA915990151
Gene: ACOX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 790538
ClinVar RCV Id: RCV000973341

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003491.1:p.Ile238Thr
CA2472301
NM_003500.4:c.713T>C