Canonical Allele Identifier: PA2829983434
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1025177
ClinVar RCV Id: RCV001325462
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Asn1688Ser
CA054360
NM_021055.3:c.5063A>G