Canonical Allele Identifier: PA2829971253
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535937

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Tyr155Cys
CA052014
NM_021055.3:c.464A>G