Allele Registry

Canonical Allele Identifier: PA2826558453

Gene: SDHD HGNC NCBI

ClinVar RCV:

RCV001016589

ClinVar Variation:

821802

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263433.1:p.Tyr54dup	CA070992 NM_001276504.2:c.161_163dup