Canonical Allele Identifier: PA2825439559
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1721813
ClinVar RCV Id: RCV002295049

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Leu1677Val
CA394314564
NM_001077183.3:c.5029C>G