Canonical Allele Identifier: PA2499262905
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 999196

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002991.2:p.Ala148Thr
CA338273338
NM_003000.3:c.442G>A