Allele Registry

Canonical Allele Identifier: PA2826558408

Gene: SDHD HGNC NCBI

ClinVar RCV:

RCV000505381

RCV001857228

ClinVar Variation:

438435

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263433.1:p.Leu41Arg	CA382617293 NM_001276504.2:c.122T>G