Canonical Allele Identifier: PA188616
Gene: SDHA HGNC NCBI

Linked Data

ClinVar Variation Id: 160358
ClinVar RCV Id: RCV000148027 RCV000163558 RCV000464783 RCV000762143 RCV000765834 RCV001824123 RCV003474794
ClinVar Variation Id: 568815
ClinVar RCV Id: RCV000689287 RCV004026322 RCV004026321
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004159.2:p.Arg585Trp
CA188615
NM_004168.4:c.1753C>T
CA891842547
NM_004168.4:c.1752_1753delinsGT