Allele Registry

Canonical Allele Identifier: PA2826558742

Gene: SDHD HGNC NCBI

ClinVar RCV:

RCV000497964

RCV000505346

RCV000569506

RCV002230973

ClinVar Variation:

431847

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263435.1:p.His50Asp	CA382617089 NM_001276506.2:c.148C>G