Canonical Allele Identifier: PA106091
Gene: NDUFS8 HGNC NCBI

Linked Data

ClinVar Variation Id: 7512
ClinVar RCV Id: RCV000007942 RCV000426335
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002487.1:p.Arg102His
CA118854
NM_002496.4:c.305G>A