Canonical Allele Identifier: PA2829412681
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 824350
ClinVar RCV Id: RCV001021382 RCV001861019
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.Ala130Gly
CA382619151
NM_003002.4:c.389C>G