Canonical Allele Identifier: PA2825577104
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238066

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Val1595Ile
CA052943
NM_001114382.3:c.4783G>A