Canonical Allele Identifier: PA2828094598
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_001350457.1:p.Ile1471Ser
CA394304696
NM_001363528.2:c.4412T>G