Canonical Allele Identifier: PA658665241
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 459172

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002991.2:p.Lys261Thr
CA338268983
NM_003000.3:c.782A>C