Allele Registry

Canonical Allele Identifier: PA2825799153

Gene: COQ8B HGNC NCBI

ClinVar RCV:

RCV000077754

ClinVar Variation:

91846

HGVS (amino-acid)	Matching Registered Transcripts
NP_001136027.1:p.Asp245Gly	CA145472 NM_001142555.3:c.734A>G