Canonical Allele Identifier: PA2827010354
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49949

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Ser1608Pro
CA022058
NM_001318829.2:c.4822T>C