Canonical Allele Identifier: PA2827013185
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406003

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Arg480Gln
CA035970
NM_001318831.2:c.1439G>A