Canonical Allele Identifier: PA2829983743
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_066399.2:p.Glu1713_Ala1716delinsLeuGlnIle
CA2580091180
NM_021055.3:c.5137_5147delinsCTTCAGAT