Canonical Allele Identifier: PA2829982647
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468126
ClinVar RCV Id: RCV000545542 RCV004024053
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Thr1618Asn
CA394309184
NM_021055.3:c.4853C>A