Canonical Allele Identifier: PA2827010633
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3069892
ClinVar RCV Id: RCV004009924
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Leu1681_Ile1682insHisLeuLeuGlyGlyGlyLeu
CA2825002357
NM_001318829.2:c.5042_5043insTCATCTCCTCGGTGGAGGACT