Canonical Allele Identifier: PA2825438431
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50124

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Arg1371Gln
CA020250
NM_001077183.3:c.4112G>A