Canonical Allele Identifier: PA1139708201
Gene: NDUFS4 HGNC NCBI

Linked Data

ClinVar Variation Id: 906327
ClinVar RCV Id: RCV001155411 RCV001155412 RCV002559496
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002486.1:p.Ser26Phe
CA3264146
NM_002495.4:c.77C>T