Canonical Allele Identifier: PA2829978308
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1010404
ClinVar RCV Id: RCV001308024
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Thr1025Asn
CA394285777
NM_021055.3:c.3074C>A