Canonical Allele Identifier: PA916023340
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468197

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Glu343Lys
CA276776600
NM_001318832.2:c.1027G>A