Canonical Allele Identifier: PA2828420226
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 954178

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Glu1301Gly
CA394299251
NM_001370405.1:c.3902A>G