Canonical Allele Identifier: PA2827012912
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 623238
ClinVar RCV Id: RCV000761363
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Leu412Pro
CA394273013
NM_001318831.2:c.1235T>C