Canonical Allele Identifier: PA2828094959
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 197025

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.His1574Pro
CA021276
NM_001363528.2:c.4721A>C