Canonical Allele Identifier: PA2829971329
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468130

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Trp167Cys
CA053524
NM_021055.3:c.501G>C
CA394309159
NM_021055.3:c.501G>T