Canonical Allele Identifier: PA2829974331
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65184

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Ala607Ser
CA015864
NM_021055.3:c.1819G>T