Canonical Allele Identifier: PA169367
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 18454
ClinVar RCV Id: RCV000013634 RCV000132167 RCV000505751 RCV000505378 RCV000627753 RCV003473111
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002991.2:p.Val140Phe
CA015853
NM_003000.3:c.418G>T