Canonical Allele Identifier: PA2827020486
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65301

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Thr1567Ile
CA021153
NM_001318832.2:c.4700C>T