Canonical Allele Identifier: PA2580277407
Gene: NDUFS8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1946433
ClinVar RCV Id: RCV002658899
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002487.1:p.Asn184Ile
CA381569840
NM_002496.4:c.551A>T