Canonical Allele Identifier: PA2826558608
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 412514
ClinVar RCV Id: RCV001011375 RCV002525628
ClinVar Variation Id: 1771773
ClinVar RCV Id: RCV002389250 RCV002509839 RCV003774307
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263435.1:p.Trp5Arg
CA070681
NM_001276506.2:c.13T>C
CA382616643
NM_001276506.2:c.13T>A