Canonical Allele Identifier: PA2828093285
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468013

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Val1096Ile
CA046764
NM_001363528.2:c.3286G>A