Canonical Allele Identifier: PA2827020963
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49962
ClinVar RCV Id: RCV000043229 RCV003311673
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Leu1688Pro
CA022245
NM_001318832.2:c.5063T>C