Canonical Allele Identifier: PA2825438670
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 12401

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Gln1436Pro
CA020573
NM_001077183.3:c.4307A>C