Canonical Allele Identifier: PA891857628
Gene: COQ8A HGNC NCBI

Linked Data

ClinVar Variation Id: 585374
ClinVar RCV Id: RCV000710474
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_064632.2:p.Asp407Glu
CA345054268
NM_020247.5:c.1221C>A
CA345054269
NM_020247.5:c.1221C>G