Canonical Allele Identifier: PA2828095569
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 449819
ClinVar RCV Id: RCV001023976 RCV001204908 RCV001696827
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Tyr1722Cys
CA055219
NM_001363528.2:c.5165A>G