Canonical Allele Identifier: PA2825437229
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406049
ClinVar RCV Id: RCV000467462

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Thr1024Pro
CA16615089
NM_001077183.3:c.3070A>C