Canonical Allele Identifier: PA2828418708
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406086
ClinVar RCV Id: RCV000458545 RCV002257697 RCV002291628 RCV003463868
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Glu845Gly
CA039405
NM_001370405.1:c.2534A>G