Canonical Allele Identifier: PA122708
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 12792
ClinVar RCV Id: RCV000013633 RCV000034688 RCV000122002 RCV000132153 RCV000206861 RCV000202946 RCV000282667 RCV000986263 RCV001099292 RCV001269360
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002991.2:p.Ser163Pro
CA015910
NM_003000.3:c.487T>C