Canonical Allele Identifier: PA2825572332
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535937

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Tyr155Cys
CA052014
NM_001114382.3:c.464A>G