Canonical Allele Identifier: PA2499248373
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1043681

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Thr52Ile
CA394301702
NM_001318832.2:c.155C>T