Canonical Allele Identifier: PA2827004767
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238056

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Val1444Ile
CA051988
NM_001318827.2:c.4330G>A