Canonical Allele Identifier: PA2829977596
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 135375

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Leu921Val
CA018107
NM_021055.3:c.2761C>G