Canonical Allele Identifier: PA2828057496
Gene: COQ2 HGNC NCBI

Linked Data

ClinVar Variation Id: 128828
ClinVar RCV Id: RCV000116807 RCV000676768 RCV000613316
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001345850.1:p.Val16Leu
CA288762
NM_001358921.2:c.46G>T
CA357231178
NM_001358921.2:c.46G>C