Canonical Allele Identifier: PA658819419
Gene: NDUFS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 522715
ClinVar RCV Id: RCV000625868
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004541.1:p.Ala90Thr
CA343377955
NM_004550.5:c.268G>A