Allele Registry

Canonical Allele Identifier: PA2826558903

Gene: SDHD HGNC NCBI

ClinVar RCV:

RCV000165195

RCV002228740

ClinVar Variation:

185719

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263435.1:p.His102Asn	CA016659 NM_001276506.2:c.304C>A