Canonical Allele Identifier: PA107935
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 12398
ClinVar RCV Id: RCV000013207 RCV000042452
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Leu717Arg
CA016832
NM_000548.5:c.2150T>G