Canonical Allele Identifier: PA891861308
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 566674
ClinVar RCV Id: RCV002547102 RCV003389826
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263432.1:p.Gly69Val
CA382618914
NM_001276503.2:c.206G>T