Canonical Allele Identifier: PA2829981777
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 838523

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Ile1502Met
CA394304898
NM_021055.3:c.4506C>G