Allele Registry

Canonical Allele Identifier: PA915975189

Gene: SDHD HGNC NCBI

ClinVar RCV:

RCV001016589

ClinVar Variation:

821802

HGVS (amino-acid)	Matching Registered Transcripts
NP_002993.1:p.Tyr93dup	CA070992 NM_003002.4:c.278_280dup