Canonical Allele Identifier: PA2825576344
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405984

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Asp1383Asn
CA050657
NM_001114382.3:c.4147G>A