Canonical Allele Identifier: PA2827007772
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 536065

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Arg700Trp
CA037721
NM_001318829.2:c.2098C>T