Canonical Allele Identifier: PA2829983865
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 486631
ClinVar RCV Id: RCV000563385 RCV000644196
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.His1726Tyr
CA394315380
NM_021055.3:c.5176C>T