Canonical Allele Identifier: PA2827005348
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65364

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Leu1605Pro
CA021783
NM_001318827.2:c.4814T>C