Canonical Allele Identifier: PA264694
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65301
ClinVar RCV Id: RCV000055523 RCV000413607 RCV001854154
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Thr1623Ile
CA021153
NM_000548.5:c.4868C>T