Canonical Allele Identifier: PA2825575785
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50148

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Gly1204Glu
CA019384
NM_001114382.3:c.3611G>A