Canonical Allele Identifier: PA2828412574
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406086

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Glu845Gly
CA039405
NM_001370404.1:c.2534A>G