Canonical Allele Identifier: PA2828094751
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Leu1512Pro
CA020960
NM_001363528.2:c.4535T>C