Canonical Allele Identifier: PA2827004682
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 639390

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Gln1422Arg
CA394304325
NM_001318827.2:c.4265A>G