Canonical Allele Identifier: PA2828414103
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535968

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Leu1303Pro
CA394299288
NM_001370404.1:c.3908T>C