Canonical Allele Identifier: PA645481042
Gene: ACOX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 375691

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003491.1:p.Arg225Trp
CA2472324
NM_003500.4:c.673C>T