Canonical Allele Identifier: PA645435664
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_000539.2:p.Thr1733del
CA16615195
NM_000548.5:c.5197_5202delinsGAC
CA2575877453
NM_000548.5:c.5197_5199del