Allele Registry

Canonical Allele Identifier: PA645441145

Gene: SDHD HGNC NCBI

ClinVar RCV:

RCV000219575

RCV000986022

RCV001294091

RCV002229212

RCV002282052

RCV003475006

ClinVar Variation:

230274

HGVS (amino-acid)	Matching Registered Transcripts
NP_002993.1:p.Leu107Arg	CA10579346 NM_003002.4:c.320T>G