Canonical Allele Identifier: PA118856
Gene: NDUFS8 HGNC NCBI

Linked Data

ClinVar Variation Id: 7513
ClinVar RCV Id: RCV000007943
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002487.1:p.Pro85Leu
CA118855
NM_002496.4:c.254C>T