Canonical Allele Identifier: PA2828414673
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1741247
ClinVar RCV Id: RCV002340027
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Phe1466Ser
CA394302858
NM_001370404.1:c.4397T>C