Allele Registry

Canonical Allele Identifier: PA2825799220

Gene: COQ8B HGNC NCBI

ClinVar RCV:

RCV000416385

RCV001091178

ClinVar Variation:

375337

HGVS (amino-acid)	Matching Registered Transcripts
NP_001136027.1:p.Arg436Gln	CA16044193 NM_001142555.3:c.1307G>A