Canonical Allele Identifier: PA2828417741
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207663
ClinVar RCV Id: RCV000644256 RCV001012959 RCV001705065 RCV003996865
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Thr584Met
CA033300
NM_001370405.1:c.1751C>T