Canonical Allele Identifier: PA2826558526
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 465236

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263433.1:p.Ala94Thr
CA382619205
NM_001276504.2:c.280G>A