Canonical Allele Identifier: PA2825438341
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207683

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Arg1342Gln
CA050701
NM_001077183.3:c.4025G>A