Canonical Allele Identifier: PA2827009658
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65304

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Ser1383Thr
CA020540
NM_001318829.2:c.4148G>C