Allele Registry

Canonical Allele Identifier: PA161989

Gene: SDHD HGNC NCBI

ClinVar RCV:

RCV000122008

RCV000569765

RCV001545828

RCV002228410

RCV003230259

RCV003997358

ClinVar Variation:

135196

HGVS (amino-acid)	Matching Registered Transcripts
NP_002993.1:p.Phe34Cys	CA016754 NM_003002.4:c.101T>G