Allele Registry

Canonical Allele Identifier: PA916006168

Gene: SDHD HGNC NCBI

ClinVar RCV:

RCV000856585

RCV002536208

RCV004002908

ClinVar Variation:

694526

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263433.1:p.Tyr75His	CA382618845 NM_001276504.2:c.223T>C