Canonical Allele Identifier: PA2828094001
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 135386

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Arg1303Gln
CA019956
NM_001363528.2:c.3908G>A