Canonical Allele Identifier: PA2828057669
Gene: COQ2 HGNC NCBI

Linked Data

ClinVar Variation Id: 214218
ClinVar RCV Id: RCV000200819 RCV001853171
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001345850.1:p.Asn367Ser
CA325402
NM_001358921.2:c.1100A>G