Canonical Allele Identifier: PA2827004596
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 12401

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Gln1400Pro
CA020573
NM_001318827.2:c.4199A>C