Canonical Allele Identifier: PA2826558793
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 1399449
ClinVar RCV Id: RCV001917685
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263435.1:p.Thr67Ala
CA382617211
NM_001276506.2:c.199A>G
CA658658102
NM_001276506.2:c.199_201delinsGCC