Canonical Allele Identifier: PA2828711048
Gene: NDUFS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 214795
ClinVar RCV Id: RCV000725777 RCV001001527 RCV001100725 RCV002515415
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364228.1:p.His380Asp
CA321716
NM_001377299.1:c.1138C>G