Canonical Allele Identifier: PA2826977304
Gene: NDUFS4 HGNC NCBI

Linked Data

ClinVar Variation Id: 214817
ClinVar RCV Id: RCV000198881 RCV000295911 RCV000329830 RCV000660466 RCV002517243 RCV003947635
ClinVar Variation Id: 2189938
ClinVar RCV Id: RCV002611937
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304980.1:p.Ser5Pro
CA323413
NM_001318051.2:c.13T>C
CA2580073315
NM_001318051.2:c.12_13delinsCC