Canonical Allele Identifier: PA2828419272
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406049
ClinVar RCV Id: RCV000467462
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Thr1025Pro
CA16615089
NM_001370405.1:c.3073A>C