Canonical Allele Identifier: PA2828421568
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1039113
ClinVar RCV Id: RCV001342520 RCV003238861
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Ala1673Val
CA394312611
NM_001370405.1:c.5018C>T