Canonical Allele Identifier: PA2825576859
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238056

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Val1524Ile
CA051988
NM_001114382.3:c.4570G>A