Canonical Allele Identifier: PA2828057541
Gene: COQ2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2008119
ClinVar RCV Id: RCV002833632

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001345850.1:p.Trp109Arg
CA357230610
NM_001358921.2:c.325T>A
CA357230612
NM_001358921.2:c.325T>C