Canonical Allele Identifier: PA2826558275
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 1118555
ClinVar RCV Id: RCV002237171

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263432.1:p.Gln84Pro
CA382619197
NM_001276503.2:c.251A>C