Canonical Allele Identifier: PA2828094205
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468077

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Ser1365Leu
CA050780
NM_001363528.2:c.4094C>T