Canonical Allele Identifier: PA2828057552
Gene: COQ2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1900491
ClinVar RCV Id: RCV002583051

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001345850.1:p.Thr128Ser
CA357230486
NM_001358921.2:c.383C>G
CA357230488
NM_001358921.2:c.382A>T