Canonical Allele Identifier: PA2829980743
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468071
ClinVar RCV Id: RCV000540815 RCV001672838 RCV003999309 RCV002330897
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Arg1366Gly
CA276753368
NM_021055.3:c.4096C>G