Canonical Allele Identifier: PA2828093433
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 135380

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Thr1138Met
CA019264
NM_001363528.2:c.3413C>T