Canonical Allele Identifier: PA2825577121
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65301

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Thr1600Ile
CA021153
NM_001114382.3:c.4799C>T