Canonical Allele Identifier: PA2828095221
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65364

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Leu1642Pro
CA021783
NM_001363528.2:c.4925T>C