Canonical Allele Identifier: PA2828412242
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207726
ClinVar RCV Id: RCV000189995 RCV000563688 RCV001086435
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Thr746Ile
CA037685
NM_001370404.1:c.2237C>T