Canonical Allele Identifier: PA2827016617
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1478025

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Ala1538Thr
CA394315690
NM_001318831.2:c.4612G>A