Canonical Allele Identifier: PA2828420867
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 639390

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Gln1482Arg
CA394304325
NM_001370405.1:c.4445A>G