Canonical Allele Identifier: PA2827016033
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 197025

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.His1396Pro
CA021276
NM_001318831.2:c.4187A>C