Allele Registry

Canonical Allele Identifier: PA105219

Gene: COQ8A HGNC NCBI

ClinVar RCV:

RCV000003828

ClinVar Variation:

3643

HGVS (amino-acid)	Matching Registered Transcripts
NP_064632.2:p.Tyr514Cys	CA116406 NM_020247.5:c.1541A>G