Canonical Allele Identifier: PA2828412978
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406089
ClinVar RCV Id: RCV000475335 RCV000761103 RCV002436402
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Asp969Gly
CA16615087
NM_001370404.1:c.2906A>G