Canonical Allele Identifier: PA645494797
Gene: NDUFS8 HGNC NCBI

Linked Data

ClinVar Variation Id: 429611
ClinVar RCV Id: RCV000493719
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002487.1:p.Asp146Asn
CA6146533
NM_002496.4:c.436G>A