Canonical Allele Identifier: PA2828093901
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1064083
ClinVar RCV Id: RCV001374006
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Ser1275Asn
CA394299199
NM_001363528.2:c.3824G>A