Allele Registry

Canonical Allele Identifier: PA1139698270

Gene: SDHD HGNC NCBI

ClinVar Allele:

926123

ClinVar RCV:

RCV002241296

ClinVar Variation:

950869

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263433.1:p.His63Pro	CA382617414 NM_001276504.2:c.188A>C