Canonical Allele Identifier: PA2829982298
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 838362

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Met1572Arg
CA394308151
NM_021055.3:c.4715T>G