Canonical Allele Identifier: PA2828419686
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 135380

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Thr1138Met
CA019264
NM_001370405.1:c.3413C>T