Canonical Allele Identifier: PA1139708289
Gene: NDUFS8 HGNC NCBI

Linked Data

ClinVar Variation Id: 884038

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002487.1:p.Gly192Arg
CA381570056
NM_002496.4:c.574G>A
CA381570058
NM_002496.4:c.574G>C