Canonical Allele Identifier: PA2827009674
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 12401

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Gln1388Pro
CA020573
NM_001318829.2:c.4163A>C