Canonical Allele Identifier: PA2826977304
Gene: NDUFS4 HGNC NCBI

Linked Data

ClinVar Variation Id: 214817
ClinVar Variation Id: 2189938
ClinVar RCV Id: RCV002611937

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