Canonical Allele Identifier: PA916006122
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 566026
ClinVar RCV Id: RCV002544721 RCV004004233 RCV003965435
ClinVar Variation Id: 1513960
ClinVar RCV Id: RCV002026438
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263432.1:p.Trp81Cys
CA382619147
NM_001276503.2:c.243G>C
CA382619148
NM_001276503.2:c.243G>T