Canonical Allele Identifier: PA2828095377
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1721813
ClinVar RCV Id: RCV002295049

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Leu1678Val
CA394314564
NM_001363528.2:c.5032C>G