Allele Registry

Canonical Allele Identifier: PA161991

Gene: SDHD HGNC NCBI

Linked Data

ClinVar RCV:

RCV000122010

RCV000508222

RCV000562051

RCV000568887

RCV001328335

RCV002230195

RCV002515893

RCV003153649

RCV003476141

RCV004002008

ClinVar Variation:

135198

412501

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_002993.1:p.Leu85Phe	CA016696 NM_003002.4:c.255G>T CA070935 NM_003002.4:c.255G>C