Canonical Allele Identifier: PA2828412771
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 12405

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Arg905Gly
CA017936
NM_001370404.1:c.2713C>G