Canonical Allele Identifier: PA658665101
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 480839

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002991.2:p.Asp161Gly
CA18665939
NM_003000.3:c.482A>G