Canonical Allele Identifier: PA2825575485
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468005
ClinVar Variation Id: 578164

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Val1120Leu
CA276746154
NM_001114382.3:c.3358G>T
CA394286664
NM_001114382.3:c.3358G>C