Canonical Allele Identifier: PA2827010121
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65215

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Ser1538Pro
CA021390
NM_001318829.2:c.4612T>C