Canonical Allele Identifier: PA2825438132
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535968

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Leu1280Pro
CA394299288
NM_001077183.3:c.3839T>C