Canonical Allele Identifier: PA2827012585
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405944
ClinVar RCV Id: RCV000471506 RCV001012244 RCV001564370
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Ser326Asn
CA031083
NM_001318831.2:c.977G>A