Canonical Allele Identifier: PA916003719
Gene: NDUFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 190449
ClinVar RCV Id: RCV000170569

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186913.1:p.Val267Gly
CA274773
NM_001199984.2:c.800T>G