Canonical Allele Identifier: PA645494784
Gene: NDUFS8 HGNC NCBI

Linked Data

ClinVar Variation Id: 305763
ClinVar RCV Id: RCV000317408 RCV000372098
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002487.1:p.Glu45Lys
CA6146386
NM_002496.4:c.133G>A