Canonical Allele Identifier: PA2829981701
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49308
ClinVar RCV Id: RCV000042567
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Leu1491His
CA020740
NM_021055.3:c.4472T>A