Canonical Allele Identifier: PA2828421802
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468157
ClinVar RCV Id: RCV000535476 RCV001821554 RCV002350300
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Ser1727Gly
CA055089
NM_001370405.1:c.5179A>G