Canonical Allele Identifier: PA2825438206
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 135386

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Arg1302Gln
CA019956
NM_001077183.3:c.3905G>A