Canonical Allele Identifier: PA2825575331
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406055

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Arg1078Gln
CA044900
NM_001114382.3:c.3233G>A