Canonical Allele Identifier: PA2827007724
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65222

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Leu684Val
CA016903
NM_001318829.2:c.2050C>G