Canonical Allele Identifier: PA2828411886
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1406765
ClinVar RCV Id: RCV001915976
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Gly654Arg
CA394273606
NM_001370404.1:c.1960G>C