Allele Registry

Canonical Allele Identifier: PA1139698294

Gene: SDHD HGNC NCBI

ClinVar RCV:

RCV001812309

RCV002451642

ClinVar Variation:

993407

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263433.1:p.Tyr75Asp	CA382618847 NM_001276504.2:c.223T>G