Canonical Allele Identifier: PA161990
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 135197
ClinVar RCV Id: RCV000122009 RCV000130895 RCV001546458 RCV002228625 RCV003398736 RCV003474733
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.Tyr93Cys
CA016634
NM_003002.4:c.278A>G