Canonical Allele Identifier: PA2827017234
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49896

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Cys255Arg
CA022889
NM_001318832.2:c.763T>C