Canonical Allele Identifier: PA2827018827
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 536003

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Arg1094Gln
CA046441
NM_001318832.2:c.3281G>A