Canonical Allele Identifier: PA277530
Gene: NDUFS8 HGNC NCBI

Linked Data

ClinVar Variation Id: 216970
ClinVar RCV Id: RCV000200148 RCV001853220
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002487.1:p.Lys115Glu
CA277529
NM_002496.4:c.343A>G