Canonical Allele Identifier: PA2828419028
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535970
ClinVar RCV Id: RCV000644215 RCV001016700
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Glu942Gly
CA276742132
NM_001370405.1:c.2825A>G