Allele Registry

Canonical Allele Identifier: PA645441150

Gene: SDHD HGNC NCBI

ClinVar Allele:

398070

ClinVar RCV:

RCV000565076

RCV001591105

RCV002230665

RCV003325203

RCV003476144

ClinVar Variation:

412515

HGVS (amino-acid)	Matching Registered Transcripts
NP_002993.1:p.Val111Ile	CA071246 NM_003002.4:c.331G>A