Canonical Allele Identifier: PA2827010088
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 197025

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.His1525Pro
CA021276
NM_001318829.2:c.4574A>C