Canonical Allele Identifier: PA2825577623
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49365

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Leu1727Phe
CA022293
NM_001114382.3:c.5179C>T