Canonical Allele Identifier: PA2829976878
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 387803

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Leu843Pro
CA16606932
NM_021055.3:c.2528T>C