Canonical Allele Identifier: PA916023187
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535920

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Ile55Thr
CA394301782
NM_001318832.2:c.164T>C