Canonical Allele Identifier: PA2828418693
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237994
ClinVar RCV Id: RCV000227059 RCV000277301 RCV002450674 RCV004532846
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Val841Ile
CA10583310
NM_001370405.1:c.2521G>A