Canonical Allele Identifier: PA2827013947
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1516394

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Pro703Thr
CA394279461
NM_001318831.2:c.2107C>A