Canonical Allele Identifier: PA2828414176
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 135386

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Arg1325Gln
CA019956
NM_001370404.1:c.3974G>A