Canonical Allele Identifier: PA2828413831
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3064495
ClinVar RCV Id: RCV003989035
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Ser1225Cys
CA394293617
NM_001370404.1:c.3674C>G