Canonical Allele Identifier: PA2828090543
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 374159

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Val296Met
CA16043501
NM_001363528.2:c.886G>A