Canonical Allele Identifier: PA2828094466
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 12401

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Gln1437Pro
CA020573
NM_001363528.2:c.4310A>C