Canonical Allele Identifier: PA2826558547
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 1739553
ClinVar RCV Id: RCV002331890 RCV003094637
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263433.1:p.Tyr105_His106del
CA2580083536
NM_001276504.2:c.313_318del