Canonical Allele Identifier: PA2828093911
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207750

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Glu1278Lys
CA050233
NM_001363528.2:c.3832G>A