Canonical Allele Identifier: PA2825572362
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 663005

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Phe163Ser
CA394309071
NM_001114382.3:c.488T>C