Canonical Allele Identifier: PA2828094264
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468083

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Pro1384Ala
CA050903
NM_001363528.2:c.4150C>G