Canonical Allele Identifier: PA2828421726
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 318336
ClinVar RCV Id: RCV000373763
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Glu1709Gly
CA10643155
NM_001370405.1:c.5126A>G