Canonical Allele Identifier: PA2829983610
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49471

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Arg1700Trp
CA022213
NM_021055.3:c.5098C>T