Canonical Allele Identifier: PA2828091588
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1460814

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Ile606Met
CA394272983
NM_001363528.2:c.1818C>G