Canonical Allele Identifier: PA2573227439
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 1379951
ClinVar RCV Id: RCV001892128

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002991.2:p.Ser239Pro
CA338270249
NM_003000.3:c.715T>C