Canonical Allele Identifier: PA2828409817
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1043681

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Thr41Ile
CA394301702
NM_001370404.1:c.122C>T