Canonical Allele Identifier: PA2825577379
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65146

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Met1668Thr
CA021670
NM_001114382.3:c.5003T>C