Canonical Allele Identifier: PA319982
Gene: NDUFS7 HGNC NCBI

Linked Data

ClinVar Variation Id: 214834
ClinVar RCV Id: RCV000195624 RCV002282032
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077718.3:p.Arg115Cys
CA319981
NM_024407.5:c.343C>T