Canonical Allele Identifier: PA2828409791
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 971297

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Glu32Lys
CA394301415
NM_001370404.1:c.94G>A