Canonical Allele Identifier: PA2827013887
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237999
ClinVar RCV Id: RCV000232046
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Gln683Glu
CA10583314
NM_001318831.2:c.2047C>G