Canonical Allele Identifier: PA2827005469
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468147
ClinVar RCV Id: RCV000550602 RCV002341373 RCV000604770 RCV003999327 RCV004538003
ClinVar Variation Id: 2806460
ClinVar RCV Id: RCV003627753
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Ile1632Val
CA054409
NM_001318827.2:c.4894A>G
CA2739269936
NM_001318827.2:c.4893_4894delinsCG