Canonical Allele Identifier: PA2827019424
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 448730

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Gly1269Asp
CA049827
NM_001318832.2:c.3806G>A