Allele Registry

Canonical Allele Identifier: PA916006175

Gene: SDHD HGNC NCBI

ClinVar RCV:

RCV000215839

ClinVar Variation:

231638

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263433.1:p.Tyr75Asn	CA10579347 NM_001276504.2:c.223T>A