Canonical Allele Identifier: PA2825573053
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50164

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Pro378Leu
CA013884
NM_001114382.3:c.1133C>T