Canonical Allele Identifier: PA2829973682
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207719
ClinVar RCV Id: RCV000189985 RCV001012413 RCV001088401
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Arg537His
CA031730
NM_021055.3:c.1610G>A