Canonical Allele Identifier: PA2827019150
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1733712
ClinVar RCV Id: RCV002452586
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Asp1189Tyr
CA394292119
NM_001318832.2:c.3565G>T