Canonical Allele Identifier: PA2828418696
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3232117
ClinVar RCV Id: RCV004520800
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Pro842Ala
CA394277939
NM_001370405.1:c.2524C>G