Allele Registry

Canonical Allele Identifier: PA2826558866

Gene: SDHD HGNC NCBI

ClinVar RCV:

RCV000171136

RCV000186596

ClinVar Variation:

180590

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263435.1:p.Asp92Gly	CA016709 NM_001276506.2:c.275A>G