Allele Registry

Canonical Allele Identifier: PA2580271641

Gene: SDHD HGNC NCBI

ClinVar RCV:

RCV002576552

ClinVar Variation:

1900919

HGVS (amino-acid)	Matching Registered Transcripts
NP_002993.1:p.His145Tyr	CA382619396 NM_003002.4:c.433C>T