Canonical Allele Identifier: PA2825573755
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1779692
ClinVar RCV Id: RCV002401747 RCV003512176
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Met589Thr
CA394272876
NM_001114382.3:c.1766T>C