Canonical Allele Identifier: PA2825574954
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 135375

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Leu921Val
CA018107
NM_001114382.3:c.2761C>G