Canonical Allele Identifier: PA2828094661
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 953372

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Gly1487Asp
CA394305086
NM_001363528.2:c.4460G>A