Canonical Allele Identifier: PA2825576833
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2633616

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Asp1518Gly
CA394304815
NM_001114382.3:c.4553A>G