Canonical Allele Identifier: PA2829981099
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238046
ClinVar RCV Id: RCV001082242 RCV000443899 RCV001022342
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Arg1408His
CA050956
NM_021055.3:c.4223G>A