Canonical Allele Identifier: PA2827004309
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468075
ClinVar Variation Id: 468076

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Gly1322Arg
CA050746
NM_001318827.2:c.3964G>A
CA394300730
NM_001318827.2:c.3964G>C