Canonical Allele Identifier: PA2827004055
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535968

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Leu1244Pro
CA394299288
NM_001318827.2:c.3731T>C