Canonical Allele Identifier: PA2828089962
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468024

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Leu119Arg
CA394306574
NM_001363528.2:c.356T>G