Allele Registry

Canonical Allele Identifier: PA916006199

Gene: SDHD HGNC NCBI

ClinVar RCV:

RCV002526127

RCV003999154

ClinVar Variation:

465238

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263433.1:p.Gly99Val	CA382619290 NM_001276504.2:c.296G>T