Canonical Allele Identifier: PA2825576516
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535870
ClinVar RCV Id: RCV000644088 RCV002483857
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Arg1434Trp
CA051001
NM_001114382.3:c.4300C>T