Canonical Allele Identifier: PA2828421723
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_001357334.1:p.Glu1709_Ala1712delinsLeuGlnIle
CA2580091180
NM_001370405.1:c.5125_5135delinsCTTCAGAT