Canonical Allele Identifier: PA274774
Gene: NDUFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 190449
ClinVar RCV Id: RCV000170569
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186910.1:p.Val217Gly
CA274773
NM_001199981.2:c.650T>G