Canonical Allele Identifier: PA2825576134
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207750

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Glu1321Lys
CA050233
NM_001114382.3:c.3961G>A