Canonical Allele Identifier: PA2829978573
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 486673
ClinVar RCV Id: RCV000562552 RCV001853809
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Lys1063Met
CA045694
NM_021055.3:c.3188A>T