Canonical Allele Identifier: PA2827015711
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238056

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Val1303Ile
CA051988
NM_001318831.2:c.3907G>A