Canonical Allele Identifier: PA2829981803
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49478
ClinVar RCV Id: RCV000042738
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Tyr1506Asn
CA020806
NM_021055.3:c.4516T>A