Canonical Allele Identifier: PA916023504
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 467870
ClinVar RCV Id: RCV000527111
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Leu484Val
CA394323959
NM_001318832.2:c.1450C>G