Allele Registry

Canonical Allele Identifier: PA2826558878

Gene: SDHD HGNC NCBI

ClinVar RCV:

RCV000020521

RCV001701640

RCV002433463

ClinVar Variation:

21351

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263435.1:p.Leu95Pro	CA016647 NM_001276506.2:c.284T>C