Canonical Allele Identifier: PA2827011377
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207726
ClinVar RCV Id: RCV000189995 RCV000563688 RCV001086435
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Thr697Ile
CA037685
NM_001318829.2:c.2090C>T