Canonical Allele Identifier: PA2825439083
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1721577
ClinVar RCV Id: RCV002300532
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Ala1550Asp
CA394308214
NM_001077183.3:c.4649C>A