Canonical Allele Identifier: PA645441018
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_002993.1:p.Trp5Arg
CA070681
NM_003002.4:c.13T>C
CA382616643
NM_003002.4:c.13T>A