Canonical Allele Identifier: PA891861307
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 581877
ClinVar RCV Id: RCV002534446
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263432.1:p.Lys61Arg
CA382618786
NM_001276503.2:c.182A>G