Canonical Allele Identifier: PA2827005666
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1440541
ClinVar RCV Id: RCV001978883

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Pro1678Thr
CA394315676
NM_001318827.2:c.5032C>A