Canonical Allele Identifier: PA2829412621
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 1717756
ClinVar RCV Id: RCV002297781
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.Asp113His
CA382618834
NM_003002.4:c.337G>C