Allele Registry

Canonical Allele Identifier: PA1139698273

Gene: SDHD HGNC NCBI

ClinVar RCV:

RCV002240202

RCV002445259

ClinVar Variation:

846101

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263433.1:p.His63Tyr	CA382617413 NM_001276504.2:c.187C>T