Canonical Allele Identifier: PA2825799105
Gene: COQ8B HGNC NCBI

Linked Data

ClinVar Variation Id: 1921318
ClinVar RCV Id: RCV002608786

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136027.1:p.Ala175Val
CA405964127
NM_001142555.3:c.524C>T