Canonical Allele Identifier: PA2827019012
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 184243

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Glu1146Lys
CA019256
NM_001318832.2:c.3436G>A