Canonical Allele Identifier: PA2826558872
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 6905
ClinVar RCV Id: RCV000007314 RCV002433446
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263435.1:p.Tyr93del
CA016628
NM_001276506.2:c.278_280del
CA2615985385
NM_001276506.2:c.276_278del