Allele Registry

Canonical Allele Identifier: PA2826558319

Gene: SDHD HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000007299

RCV000007300

RCV000007302

RCV000034697

RCV000122006

RCV000162470

RCV000988742

RCV001807000

RCV002228001

ClinVar Variation:

6895

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263433.1:p.Gly12Ser	CA016980 NM_001276504.2:c.34G>A