Canonical Allele Identifier: PA2827019119
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1483061
ClinVar RCV Id: RCV002025337

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Leu1179Met
CA394291753
NM_001318832.2:c.3535C>A