Canonical Allele Identifier: PA2825572785
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 374159

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Val296Met
CA16043501
NM_001114382.3:c.886G>A