Canonical Allele Identifier: PA2829982946
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65146

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Met1648Thr
CA021670
NM_021055.3:c.4943T>C