Canonical Allele Identifier: PA916024000
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50114
ClinVar RCV Id: RCV000043381
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Leu927Arg
CA018075
NM_001318832.2:c.2780T>G