Canonical Allele Identifier: PA916023112
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 135380

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Thr937Met
CA019264
NM_001318831.2:c.2810C>T