Allele Registry

Canonical Allele Identifier: PA916006202

Gene: SDHD HGNC NCBI

ClinVar RCV:

RCV000167450

RCV000478572

RCV002228995

ClinVar Variation:

187700

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263433.1:p.Gly99Arg	CA017004 NM_001276504.2:c.295G>A CA382619281 NM_001276504.2:c.295G>C