Canonical Allele Identifier: PA2827012023
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 135380

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Thr1089Met
CA019264
NM_001318829.2:c.3266C>T