Allele Registry

Canonical Allele Identifier: PA2826558585

Gene: SDHD HGNC NCBI

ClinVar Allele:

165953

ClinVar RCV:

RCV000144172

RCV000454533

RCV000505355

RCV000994727

RCV001023072

RCV002228513

ClinVar Variation:

156154

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263433.1:p.Leu120_Ter121insLeuProPhe	CA016726 NM_001276504.2:c.362G>T