Canonical Allele Identifier: PA2580380413
Gene: COQ2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2008119
ClinVar RCV Id: RCV002833632

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056512.5:p.Trp159Arg
CA357230610
NM_015697.9:c.475T>A
CA357230612
NM_015697.9:c.475T>C