Canonical Allele Identifier: PA2827009577
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207685

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Glu1361Lys
CA051101
NM_001318829.2:c.4081G>A