Canonical Allele Identifier: PA2829982253
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468115

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Tyr1565Cys
CA052633
NM_021055.3:c.4694A>G