Canonical Allele Identifier: PA2573222784
Gene: NDUFS8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1477397
ClinVar RCV Id: RCV001998349
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002487.1:p.Thr127Ile
CA6146512
NM_002496.4:c.380C>T