Canonical Allele Identifier: PA2827016684
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_001305760.1:p.Leu1552_Ile1553insHisLeuLeuGlyGlyGlyLeu
CA2825002357
NM_001318831.2:c.4655_4656insTCATCTCCTCGGTGGAGGACT