Canonical Allele Identifier: PA2828090766
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535916

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Glu366Gln
CA276776700
NM_001363528.2:c.1096G>C