Canonical Allele Identifier: PA916023236
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535937

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Tyr166Cys
CA052014
NM_001318832.2:c.497A>G