Canonical Allele Identifier: PA2829979056
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 450949
ClinVar RCV Id: RCV000520176 RCV001020414 RCV001085805 RCV004003619
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Pro1119Leu
CA047132
NM_021055.3:c.3356C>T