Canonical Allele Identifier: PA2828094958
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49333

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.His1574Tyr
CA021270
NM_001363528.2:c.4720C>T