Canonical Allele Identifier: PA2825577599
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1721813
ClinVar RCV Id: RCV002295049

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Leu1721Val
CA394314564
NM_001114382.3:c.5161C>G