Canonical Allele Identifier: PA2825439720
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1478025

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Ala1715Thr
CA394315690
NM_001077183.3:c.5143G>A