Canonical Allele Identifier: PA2827005834
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65108

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Ile15Val
CA016191
NM_001318829.2:c.43A>G