Canonical Allele Identifier: PA2828413588
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406069
ClinVar RCV Id: RCV000570432 RCV000461845 RCV001662421 RCV004000712
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Ala1151Val
CA047499
NM_001370404.1:c.3452C>T