Canonical Allele Identifier: PA915974229
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 648617
ClinVar RCV Id: RCV000803380

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002991.2:p.Met103Ile
CA338275043
NM_003000.3:c.309G>T
CA338275045
NM_003000.3:c.309G>C
CA338275048
NM_003000.3:c.309G>A