Canonical Allele Identifier: PA2827005100
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_001305756.1:p.Asn1540His
CA021298
NM_001318827.2:c.4618A>C