Canonical Allele Identifier: PA915974334
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 659740
ClinVar RCV Id: RCV000816787
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002991.2:p.Asp138Gly
CA338273943
NM_003000.3:c.413A>G