Canonical Allele Identifier: PA2828415964
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 486649

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Ile44Val
CA394301772
NM_001370405.1:c.130A>G