Canonical Allele Identifier: PA2828412729
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207734
ClinVar RCV Id: RCV000190005 RCV000644168 RCV002426918
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Ile893Thr
CA319484
NM_001370404.1:c.2678T>C