Canonical Allele Identifier: PA2828091935
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 226045
ClinVar RCV Id: RCV000211466 RCV000542869 RCV001580472 RCV002415885
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Val692Ile
CA036245
NM_001363528.2:c.2074G>A