Canonical Allele Identifier: PA2827004741
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2633616
ClinVar RCV Id: RCV004529305 RCV003512222
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Asp1438Gly
CA394304815
NM_001318827.2:c.4313A>G