Canonical Allele Identifier: PA2827015946
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 838362

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Met1371Arg
CA394308151
NM_001318831.2:c.4112T>G