Canonical Allele Identifier: PA213079
Gene: COQ2 HGNC NCBI

Linked Data

ClinVar Variation Id: 60539

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056512.5:p.Arg387Gln
CA213078
NM_015697.9:c.1160G>A