Canonical Allele Identifier: PA2827010669
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 536087

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Glu1690Lys
CA055360
NM_001318829.2:c.5068G>A