Canonical Allele Identifier: PA2828090118
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 663005
ClinVar RCV Id: RCV000820781 RCV001585759
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Phe163Ser
CA394309071
NM_001363528.2:c.488T>C