Canonical Allele Identifier: PA2828412565
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 387803

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Leu843Pro
CA16606932
NM_001370404.1:c.2528T>C