Canonical Allele Identifier: PA2828421604
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 935997
ClinVar RCV Id: RCV001204707 RCV002339515
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Ser1681Ile
CA394314110
NM_001370405.1:c.5042G>T