Canonical Allele Identifier: PA2827008437
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 64897

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Leu969Pro
CA018665
NM_001318829.2:c.2906T>C