Canonical Allele Identifier: PA2827020337
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Leu1522Pro
CA020960
NM_001318832.2:c.4565T>C