Canonical Allele Identifier: PA2828057632
Gene: COQ2 HGNC NCBI

Linked Data

ClinVar Variation Id: 60537
ClinVar RCV Id: RCV000054429
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001345850.1:p.Val293Ala
CA144549
NM_001358921.2:c.878T>C