Canonical Allele Identifier: PA2827013100
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2179574
ClinVar RCV Id: RCV002599171
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Ser460Gly
CA035386
NM_001318831.2:c.1378A>G