Allele Registry

Canonical Allele Identifier: PA2826558451

Gene: SDHD HGNC NCBI

ClinVar RCV:

RCV000122009

RCV000130895

RCV001546458

RCV002228625

RCV003398736

RCV003474733

ClinVar Variation:

135197

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263433.1:p.Tyr54Cys	CA016634 NM_001276504.2:c.161A>G