Canonical Allele Identifier: PA2827002906
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 135375

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Leu884Val
CA018107
NM_001318827.2:c.2650C>G