Canonical Allele Identifier: PA2827002654
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406086

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Glu808Gly
CA039405
NM_001318827.2:c.2423A>G