Canonical Allele Identifier: PA891848273
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 568517
ClinVar RCV Id: RCV002233178
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.Val71Ile
CA382617240
NM_003002.4:c.211G>A