Canonical Allele Identifier: PA2828090667
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535893

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Tyr336Cys
CA027968
NM_001363528.2:c.1007A>G