Allele Registry

Canonical Allele Identifier: PA2826558411

Gene: SDHD HGNC NCBI

ClinVar RCV:

RCV002251308

RCV003774738

ClinVar Variation:

1687625

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263433.1:p.Pro42Arg	CA382617298 NM_001276504.2:c.125C>G