Canonical Allele Identifier: PA2825576785
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 848503

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Glu1505Gln
CA394304419
NM_001114382.3:c.4513G>C