Canonical Allele Identifier: PA2828420010
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535957
ClinVar RCV Id: RCV000644199 RCV002358833 RCV002493023
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Gln1241Arg
CA276750917
NM_001370405.1:c.3722A>G