Canonical Allele Identifier: PA2827000141
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65108
ClinVar RCV Id: RCV000055320 RCV000644085 RCV001118864 RCV002408557 RCV003466927
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Ile64Val
CA016191
NM_001318827.2:c.190A>G