Allele Registry

Canonical Allele Identifier: PA2826558445

Gene: SDHD HGNC NCBI

ClinVar RCV:

RCV000171136

RCV000186596

ClinVar Variation:

180590

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263433.1:p.Asp53Gly	CA016709 NM_001276504.2:c.158A>G