Canonical Allele Identifier: PA2828421771
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468155
ClinVar RCV Id: RCV000547303 RCV000570898 RCV003403303
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Leu1720Val
CA054998
NM_001370405.1:c.5158C>G