Canonical Allele Identifier: PA2828413665
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1733630
ClinVar RCV Id: RCV002452509
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Phe1175Ser
CA394292043
NM_001370404.1:c.3524T>C