Canonical Allele Identifier: PA2826977307
Gene: NDUFS4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1912032
ClinVar RCV Id: RCV002597401

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304980.1:p.Val9Leu
CA3264128
NM_001318051.2:c.25G>C
CA359718963
NM_001318051.2:c.25G>T