Canonical Allele Identifier: PA2827004727
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1509011
ClinVar RCV Id: RCV002016530
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Ile1434Ser
CA394304696
NM_001318827.2:c.4301T>G