Canonical Allele Identifier: PA2825576446
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50124

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Arg1415Gln
CA020250
NM_001114382.3:c.4244G>A