Canonical Allele Identifier: PA2825574440
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237987
ClinVar RCV Id: RCV000234604 RCV000392158 RCV000574918 RCV001697576 RCV004532844
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Val766Met
CA038245
NM_001114382.3:c.2296G>A