Canonical Allele Identifier: PA2828711349
Gene: NDUFS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 293273
ClinVar RCV Id: RCV000386683 RCV001859752 RCV003343755
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364231.1:p.Ile113Val
CA1208536
NM_001377302.1:c.337A>G