Canonical Allele Identifier: PA2828094447
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65304

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Ser1432Thr
CA020540
NM_001363528.2:c.4295G>C