Canonical Allele Identifier: PA2829981795
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238056

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Val1504Ile
CA051988
NM_021055.3:c.4510G>A