Canonical Allele Identifier: PA2825575708
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 135380

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Thr1181Met
CA019264
NM_001114382.3:c.3542C>T