Canonical Allele Identifier: PA2827004748
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1741992

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.His1440Gln
CA051970
NM_001318827.2:c.4320C>G
CA394304854
NM_001318827.2:c.4320C>A