Canonical Allele Identifier: PA2828415965
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535920

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Ile44Thr
CA394301782
NM_001370405.1:c.131T>C