Canonical Allele Identifier: PA2825577586
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1503018

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Ala1719Val
CA394314530
NM_001114382.3:c.5156C>T