Canonical Allele Identifier: PA2828057543
Gene: COQ2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1897906
ClinVar RCV Id: RCV002573680

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001345850.1:p.Met111Ile
CA2988626
NM_001358921.2:c.333G>T
CA357230590
NM_001358921.2:c.333G>C
CA357230591
NM_001358921.2:c.333G>A