Canonical Allele Identifier: PA2828421284
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49910
ClinVar RCV Id: RCV000043177 RCV000478359
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Asn1600His
CA021298
NM_001370405.1:c.4798A>C