Canonical Allele Identifier: PA2827012783
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1432735
ClinVar RCV Id: RCV001944059
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.His382Arg
CA394272769
NM_001318831.2:c.1145A>G