Canonical Allele Identifier: PA2826558635
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 533785
ClinVar RCV Id: RCV002533254

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263435.1:p.Ala13Thr
CA382616718
NM_001276506.2:c.37G>A