Canonical Allele Identifier: PA2827006295
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 318307

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Ile198Val
CA056277
NM_001318829.2:c.592A>G