Canonical Allele Identifier: PA2825575314
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238015

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Val1073Met
CA044793
NM_001114382.3:c.3217G>A