Canonical Allele Identifier: PA2828090434
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49921

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Leu264Pro
CA022990
NM_001363528.2:c.791T>C