Canonical Allele Identifier: PA2827012421
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 467870
ClinVar RCV Id: RCV000527111
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Leu273Val
CA394323959
NM_001318831.2:c.817C>G