Allele Registry

Canonical Allele Identifier: PA118553

Gene: SDHD HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000007318

RCV000023207

RCV000034696

RCV000122007

RCV000129149

RCV000238643

RCV000988743

RCV002228009

RCV003924810

ClinVar Variation:

6909

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_002993.1:p.His50Arg	CA016777 NM_003002.4:c.149A>G