Canonical Allele Identifier: PA2825799153
Gene: COQ8B HGNC NCBI

Linked Data

ClinVar Variation Id: 91846
ClinVar RCV Id: RCV000077754

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136027.1:p.Asp245Gly
CA145472
NM_001142555.3:c.734A>G