Canonical Allele Identifier: PA2825577627
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207760

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Arg1728His
CA054581
NM_001114382.3:c.5183G>A