Canonical Allele Identifier: PA2828415076
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_001357333.1:p.Thr1579Ile
CA021153
NM_001370404.1:c.4736C>T