Canonical Allele Identifier: PA1139709300
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 965957
ClinVar RCV Id: RCV001240523 RCV002393618
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002991.2:p.Arg251Ser
CA338270003
NM_003000.3:c.753G>T
CA338270004
NM_003000.3:c.753G>C