Canonical Allele Identifier: PA2826558495
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 842426
ClinVar RCV Id: RCV001759763 RCV002240169 RCV002451174 RCV004004774
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263433.1:p.Asp79Glu
CA382618932
NM_001276504.2:c.237T>A
CA382618935
NM_001276504.2:c.237T>G