Allele Registry

Canonical Allele Identifier: PA2826558901

Gene: SDHD HGNC NCBI

ClinVar Variation Id: 6898

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263435.1:p.His102Leu	CA016665 NM_001276506.2:c.305A>T