Canonical Allele Identifier: PA2826558632
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 2151603
ClinVar RCV Id: RCV003061423

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263435.1:p.Gly12Arg
CA382616709
NM_001276506.2:c.34G>C