Canonical Allele Identifier: PA2825575513
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 536003

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Arg1127Gln
CA046441
NM_001114382.3:c.3380G>A