Canonical Allele Identifier: PA208528
Gene: COQ8A HGNC NCBI

Linked Data

ClinVar Variation Id: 210097
ClinVar RCV Id: RCV000194388 RCV001852541
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_064632.2:p.Thr511Met
CA208527
NM_020247.5:c.1532C>T