Canonical Allele Identifier: PA2828419220
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207741

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Glu1006Lys
CA319501
NM_001370405.1:c.3016G>A