Canonical Allele Identifier: PA161982
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 135192
ClinVar RCV Id: RCV000129655 RCV000122000 RCV000148867 RCV000301812 RCV000358920 RCV000513898 RCV001083041 RCV003315777
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002991.2:p.His57Arg
CA015557
NM_003000.3:c.170A>G