Canonical Allele Identifier: PA264755
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65364

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Leu1708Pro
CA021783
NM_000548.5:c.5123T>C