Allele Registry

Canonical Allele Identifier: PA2826558904

Gene: SDHD HGNC NCBI

ClinVar RCV:

RCV002240202

RCV002445259

ClinVar Variation:

846101

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263435.1:p.His102Tyr	CA382617413 NM_001276506.2:c.304C>T