Canonical Allele Identifier: PA2828420884
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468105

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Arg1486Gln
CA394304453
NM_001370405.1:c.4457G>A