Canonical Allele Identifier: PA2828417237
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65257
ClinVar RCV Id: RCV000055478 RCV000475576 RCV001010823
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Ser433Cys
CA014387
NM_001370405.1:c.1298C>G