Canonical Allele Identifier: PA2828417927
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406129
ClinVar RCV Id: RCV000460911 RCV002256251 RCV004000726
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Arg628Cys
CA034358
NM_001370405.1:c.1882C>T