Canonical Allele Identifier: PA2828421636
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 661952
ClinVar RCV Id: RCV001023722 RCV000819482
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Ile1688Thr
CA276759442
NM_001370405.1:c.5063T>C