Canonical Allele Identifier: PA2825575247
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1728211
ClinVar RCV Id: RCV002320843

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Leu1051Arg
CA394285304
NM_001114382.3:c.3152T>G