Canonical Allele Identifier: PA2827009910
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Leu1463Pro
CA020960
NM_001318829.2:c.4388T>C