Canonical Allele Identifier: PA2828415554
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1721813
ClinVar RCV Id: RCV002295049

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Leu1700Val
CA394314564
NM_001370404.1:c.5098C>G