Canonical Allele Identifier: PA2827002851
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 12405

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Arg868Gly
CA017936
NM_001318827.2:c.2602C>G