Canonical Allele Identifier: PA210092
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49325
ClinVar RCV Id: RCV000042585 RCV000201210 RCV001283509
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Ile1614del
CA021081
NM_000548.5:c.4842_4844del