Canonical Allele Identifier: PA2826558549
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 1900919
ClinVar RCV Id: RCV002576552
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263433.1:p.His106Tyr
CA382619396
NM_001276504.2:c.316C>T