Canonical Allele Identifier: PA2828416952
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406037
ClinVar RCV Id: RCV000462431 RCV002393093
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Ile346Val
CA16615037
NM_001370405.1:c.1036A>G