Canonical Allele Identifier: PA2825577638
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 565761
ClinVar RCV Id: RCV000685400 RCV002334249
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Arg1730Trp
CA054606
NM_001114382.3:c.5188C>T