Canonical Allele Identifier: PA2825438862
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 953372

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Gly1486Asp
CA394305086
NM_001077183.3:c.4457G>A