Allele Registry

Canonical Allele Identifier: PA2829901382

Gene: UQCC1 HGNC NCBI

ClinVar RCV:

RCV001641670

ClinVar Variation:

1245347

HGVS (amino-acid)	Matching Registered Transcripts
NP_060714.3:p.Arg51Gln	CA9831951 NM_018244.5:c.152G>A