Canonical Allele Identifier: PA2827004653
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468098

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Ile1415Val
CA051585
NM_001318827.2:c.4243A>G