Canonical Allele Identifier: PA2827019170
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406092
ClinVar RCV Id: RCV000475309 RCV002348295
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Gln1196Arg
CA16614724
NM_001318832.2:c.3587A>G