Canonical Allele Identifier: PA2825438847
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1519233
ClinVar RCV Id: RCV002024455

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Tyr1482His
CA394304973
NM_001077183.3:c.4444T>C