Canonical Allele Identifier: PA2826558810
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 412499
ClinVar RCV Id: RCV001800690 RCV002429558 RCV002230194
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263435.1:p.Ser73Gly
CA070865
NM_001276506.2:c.217A>G