Canonical Allele Identifier: PA2828093245
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406032

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Arg1086Cys
CA16615117
NM_001363528.2:c.3256C>T