Canonical Allele Identifier: PA2499291162
Gene: COQ8B HGNC NCBI

Linked Data

ClinVar Variation Id: 1220310
ClinVar RCV Id: RCV001592568
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079152.3:p.Gly231Arg
CA9450333
NM_024876.4:c.691G>A
CA405963904
NM_024876.4:c.691G>C