Canonical Allele Identifier: PA2828419972
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535915
ClinVar RCV Id: RCV000644144 RCV002358832 RCV004004000
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Asn1227Ser
CA394293642
NM_001370405.1:c.3680A>G