Canonical Allele Identifier: PA2827003839
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1734981
ClinVar RCV Id: RCV002353100 RCV003626714
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Leu1186Val
CA394293547
NM_001318827.2:c.3556C>G