Canonical Allele Identifier: PA107655
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 1767632

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002991.2:p.Ala43Pro
CA338228149
NM_003000.3:c.127G>C