Canonical Allele Identifier: PA2828420954
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Leu1505Pro
CA020803
NM_001370405.1:c.4514T>C