Canonical Allele Identifier: PA658666469
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_002993.1:p.Thr67Ala
CA382617211
NM_003002.4:c.199A>G
CA658658102
NM_003002.4:c.199_201delinsGCC