Allele Registry

Canonical Allele Identifier: PA2826558590

Gene: SDHD HGNC NCBI

ClinVar RCV:

RCV000485004

RCV000492287

RCV002526633

ClinVar Variation:

422629

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263435.1:p.Met1Leu