Canonical Allele Identifier: PA2828095413
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 565761

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Arg1687Trp
CA054606
NM_001363528.2:c.5059C>T