Canonical Allele Identifier: PA2827015519
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65304

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Ser1254Thr
CA020540
NM_001318831.2:c.3761G>C