Allele Registry

Canonical Allele Identifier: PA192718

Gene: SDHD HGNC NCBI

ClinVar RCV:

RCV000165195

RCV002228740

ClinVar Variation:

185719

HGVS (amino-acid)	Matching Registered Transcripts
NP_002993.1:p.His102Asn	CA016659 NM_003002.4:c.304C>A