Canonical Allele Identifier: PA2828421214
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65301

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Thr1580Ile
CA021153
NM_001370405.1:c.4739C>T