Canonical Allele Identifier: PA2828421833
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535864
ClinVar RCV Id: RCV000644075
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Pro1734Ala
CA394315679
NM_001370405.1:c.5200C>G