Canonical Allele Identifier: PA2825799106
Gene: COQ8B HGNC NCBI

Linked Data

ClinVar Variation Id: 2138297
ClinVar RCV Id: RCV003041371
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136027.1:p.Ala176Thr
CA9450339
NM_001142555.3:c.526G>A