Canonical Allele Identifier: PA2580183941
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 1734053
ClinVar RCV Id: RCV002353010
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263432.1:p.Leu75Arg
CA071312
NM_001276503.2:c.224T>G