Canonical Allele Identifier: PA2825439526
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2416226

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Tyr1669Cys
CA394314314
NM_001077183.3:c.5006A>G