Canonical Allele Identifier: PA2827020033
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65304

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Ser1442Thr
CA020540
NM_001318832.2:c.4325G>C