Canonical Allele Identifier: PA322343
Gene: NDUFS8 HGNC NCBI

Linked Data

ClinVar Variation Id: 214841
ClinVar RCV Id: RCV000197878

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002487.1:p.Gln204Leu
CA322342
NM_002496.4:c.611A>T