Canonical Allele Identifier: PA2825572706
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 480835

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Tyr274Cys
CA394313259
NM_001114382.3:c.821A>G