Allele Registry

Canonical Allele Identifier: PA645441115

Gene: SDHD HGNC NCBI

ClinVar RCV:

RCV000479419

RCV000569878

RCV002525847

ClinVar Variation:

420665

HGVS (amino-acid)	Matching Registered Transcripts
NP_002993.1:p.Asp92Val	CA16619272 NM_003002.4:c.275A>T