Canonical Allele Identifier: PA2828415875
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 639541
ClinVar RCV Id: RCV000792358

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Glu13del
CA047363
NM_001370405.1:c.37_39del
CA394300847
NM_001370405.1:c.37G>T