Canonical Allele Identifier: PA916073138
Gene: COQ8A HGNC NCBI

Linked Data

ClinVar Variation Id: 804507
ClinVar RCV Id: RCV000991497

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_064632.2:p.Thr519Ser
CA1425538
NM_020247.5:c.1556C>G
CA345055938
NM_020247.5:c.1555A>T