Canonical Allele Identifier: PA916024020
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49233

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Phe944Cys
CA018204
NM_001318832.2:c.2831T>G