Canonical Allele Identifier: PA2829984261
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3069892
ClinVar RCV Id: RCV004009924

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Leu1753_Ile1754insHisLeuLeuGlyGlyGlyLeu
CA2825002357
NM_021055.3:c.5258_5259insTCATCTCCTCGGTGGAGGACT