Canonical Allele Identifier: PA2826558270
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 3223043
ClinVar RCV Id: RCV004508398
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263432.1:p.Gly79Ala
CA382619099
NM_001276503.2:c.236G>C