Canonical Allele Identifier: PA2828420266
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468061
ClinVar RCV Id: RCV000544952 RCV001584296 RCV000764030 RCV003999303 RCV004024051
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Arg1312Gly
CA394299372
NM_001370405.1:c.3934A>G