Canonical Allele Identifier: PA2825439617
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406083

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Glu1690Lys
CA16615048
NM_001077183.3:c.5068G>A