Canonical Allele Identifier: PA2829982463
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 197025

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.His1597Pro
CA021276
NM_021055.3:c.4790A>C