Canonical Allele Identifier: PA891848316
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 566026
ClinVar RCV Id: RCV002544721 RCV004004233 RCV003965435
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.Ala130Pro
CA382619147
NM_003002.4:c.388G>C