Allele Registry

Canonical Allele Identifier: PA2826558871

Gene: SDHD HGNC NCBI

ClinVar RCV:

RCV001016589

ClinVar Variation:

821802

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263435.1:p.Tyr93dup	CA070992 NM_001276506.2:c.278_280dup