Allele Registry

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Canonical Allele Identifier: PA2826558298

Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 412514

ClinVar RCV Id: RCV001011375 RCV002525628

ClinVar Variation Id: 1771773

ClinVar RCV Id: RCV002389250 RCV002509839 RCV003774307

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263433.1:p.Trp5Arg	CA070681 NM_001276504.2:c.13T>C CA382616643 NM_001276504.2:c.13T>A