Allele Registry

Canonical Allele Identifier: PA645473960

Gene: UQCC3 HGNC NCBI

ClinVar Variation Id: 380147

HGVS (amino-acid)	Matching Registered Transcripts
NP_001078841.1:p.Gly89Ser	CA6052606 NM_001085372.3:c.265G>A