Canonical Allele Identifier: PA2825574260
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 380717

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Ser716Phe
CA036848
NM_001114382.3:c.2147C>T