Canonical Allele Identifier: PA2825577830
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3069892
ClinVar RCV Id: RCV004009924

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Leu1773_Ile1774insHisLeuLeuGlyGlyGlyLeu
CA2825002357
NM_001114382.3:c.5318_5319insTCATCTCCTCGGTGGAGGACT