Canonical Allele Identifier: PA2741896501
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 2945347
ClinVar RCV Id: RCV003801001
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002991.2:p.Phe238Val
CA338270256
NM_003000.3:c.712T>G