Canonical Allele Identifier: PA2825576256
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65358

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Ser1356Leu
CA019991
NM_001114382.3:c.4067C>T