Canonical Allele Identifier: PA2828093513
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50148
ClinVar RCV Id: RCV000043416 RCV000201026 RCV000414012
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Gly1161Glu
CA019384
NM_001363528.2:c.3482G>A