Canonical Allele Identifier: PA2827007066
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 64901

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Leu479Pro
CA015160
NM_001318829.2:c.1436T>C