Allele Registry

Canonical Allele Identifier: PA2829412582

Gene: SDHD HGNC NCBI

ClinVar RCV:

RCV002241296

ClinVar Variation:

950869

HGVS (amino-acid)	Matching Registered Transcripts
NP_002993.1:p.His102Pro	CA382617414 NM_003002.4:c.305A>C