Canonical Allele Identifier: PA2827008191
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 12405

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Arg856Gly
CA017936
NM_001318829.2:c.2566C>G