Canonical Allele Identifier: PA2828417520
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2626418
ClinVar RCV Id: RCV003382398
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Thr521Ile
CA394326548
NM_001370405.1:c.1562C>T