Canonical Allele Identifier: PA2828413133
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65377

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Thr1024Ile
CA018678
NM_001370404.1:c.3071C>T