Canonical Allele Identifier: PA2829983592
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1503018

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Ala1699Val
CA394314530
NM_021055.3:c.5096C>T