Canonical Allele Identifier: PA915974497
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 826367

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002991.2:p.Met213Leu
CA089681
NM_003000.3:c.637A>T
CA338270933
NM_003000.3:c.637A>C