Allele Registry

Canonical Allele Identifier: PA2580478737

Gene: UQCC2 HGNC NCBI

ClinVar RCV:

RCV003223366

ClinVar Variation:

2499488

HGVS (amino-acid)	Matching Registered Transcripts
NP_115716.1:p.Arg34Gln	CA137114488 NM_032340.4:c.101G>A