Canonical Allele Identifier: PA2828420256
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238040

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Glu1308Lys
CA10583329
NM_001370405.1:c.3922G>A