Canonical Allele Identifier: PA2825576819
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1741892
ClinVar RCV Id: RCV002342459
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Ile1514Asn
CA394304697
NM_001114382.3:c.4541T>A