Canonical Allele Identifier: PA2825572494
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 184164

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Ala210Thr
CA022705
NM_001114382.3:c.628G>A