Canonical Allele Identifier: PA2825575104
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 839746

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Gly1001Val
CA043753
NM_001114382.3:c.3002G>T