Canonical Allele Identifier: PA2825576992
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 265281

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Glu1560Lys
CA10588598
NM_001114382.3:c.4678G>A