Allele Registry

Canonical Allele Identifier: PA2826558549

Gene: SDHD HGNC NCBI

ClinVar RCV:

RCV002576552

ClinVar Variation:

1900919

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263433.1:p.His106Tyr	CA382619396 NM_001276504.2:c.316C>T