Canonical Allele Identifier: PA2825572489
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65103

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Arg208Trp
CA022695
NM_001114382.3:c.622C>T