Canonical Allele Identifier: PA2826558308
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 857872
ClinVar RCV Id: RCV002240503 RCV004030500
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263433.1:p.Ser8Gly
CA382616673
NM_001276504.2:c.22A>G