Canonical Allele Identifier: PA2827019439
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535925

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Arg1273Cys
CA049839
NM_001318832.2:c.3817C>T