Canonical Allele Identifier: PA2827005565
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406083

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Glu1654Lys
CA16615048
NM_001318827.2:c.4960G>A