Canonical Allele Identifier: PA916023166
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 639541
ClinVar RCV Id: RCV000792358

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Glu24del
CA047363
NM_001318832.2:c.70_72del
CA394300847
NM_001318832.2:c.70G>T