Allele Registry

Canonical Allele Identifier: PA2829412631

Gene: SDHD HGNC NCBI

ClinVar RCV:

RCV001812309

RCV002451642

ClinVar Variation:

993407

HGVS (amino-acid)	Matching Registered Transcripts
NP_002993.1:p.Tyr114Asp	CA382618847 NM_003002.4:c.340T>G