Canonical Allele Identifier: PA2825576400
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468075
ClinVar Variation Id: 468076

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Gly1402Arg
CA050746
NM_001114382.3:c.4204G>A
CA394300730
NM_001114382.3:c.4204G>C