Canonical Allele Identifier: PA645439433
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 371795
ClinVar RCV Id: RCV000412414 RCV000571866 RCV000465994 RCV001591047 RCV003153568
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002991.2:p.Pro237Ser
CA089715
NM_003000.3:c.709C>T