Canonical Allele Identifier: PA2828410393
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65337
ClinVar RCV Id: RCV000055561 RCV001053191
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Leu219Pro
CA022749
NM_001370404.1:c.656T>C