Canonical Allele Identifier: PA2827002638
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_001305756.1:p.Val804Ile
CA10583310
NM_001318827.2:c.2410G>A