Canonical Allele Identifier: PA2827006939
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1424794
ClinVar RCV Id: RCV001924040 RCV004010903
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Glu434Gln
CA394325437
NM_001318829.2:c.1300G>C