Canonical Allele Identifier: PA2828415956
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1755126
ClinVar RCV Id: RCV002375937
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Thr41Asn
CA394301700
NM_001370405.1:c.122C>A