Canonical Allele Identifier: PA107838
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 6898
ClinVar RCV Id: RCV000007307 RCV000566289 RCV002228003
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.His102Leu
CA016665
NM_003002.4:c.305A>T