Canonical Allele Identifier: PA2826558801
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 239463
ClinVar RCV Id: RCV000505342 RCV001014431 RCV002229346
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263435.1:p.Arg70Lys
CA070846
NM_001276506.2:c.209G>A