Canonical Allele Identifier: PA2829980144
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 448730

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Gly1282Asp
CA049827
NM_021055.3:c.3845G>A