Canonical Allele Identifier: PA2825439514
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405952
ClinVar RCV Id: RCV000467027
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Thr1666del
CA16615195
NM_001077183.3:c.4996_5001delinsGAC
CA2575877453
NM_001077183.3:c.4996_4998del