Canonical Allele Identifier: PA2828419297
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 954021
ClinVar RCV Id: RCV001226403
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Thr1032Asn
CA394285972
NM_001370405.1:c.3095C>A