Canonical Allele Identifier: PA2827013144
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65383

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Pro470Leu
CA016425
NM_001318831.2:c.1409C>T