Canonical Allele Identifier: PA2827005556
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1917216
ClinVar RCV Id: RCV002598099
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Glu1653_Ala1656delinsLeuGlnIle
CA2580091180
NM_001318827.2:c.4957_4967delinsCTTCAGAT