Canonical Allele Identifier: PA2827016326
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1000279

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Met1471Thr
CA054058
NM_001318831.2:c.4412T>C