Canonical Allele Identifier: PA2825577653
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 318336
ClinVar RCV Id: RCV000373763

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Glu1733Gly
CA10643155
NM_001114382.3:c.5198A>G