Allele Registry

Canonical Allele Identifier: PA2829412744

Gene: SDHD HGNC NCBI

ClinVar RCV:

RCV000144172

RCV000454533

RCV000505355

RCV000994727

RCV001023072

RCV002228513

ClinVar Variation:

156154

HGVS (amino-acid)	Matching Registered Transcripts
NP_002993.1:p.Leu159_Ter160insLeuProPhe	CA016726 NM_003002.4:c.479G>T