Canonical Allele Identifier: PA2828094155
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535982

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Arg1351Trp
CA050704
NM_001363528.2:c.4051C>T