Canonical Allele Identifier: PA2825437560
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49755

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Arg1115Gln
CA019197
NM_001077183.3:c.3344G>A