Canonical Allele Identifier: PA2825572945
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406037

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Ile346Val
CA16615037
NM_001114382.3:c.1036A>G