Canonical Allele Identifier: PA2827013362
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 231749

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Pro527Leu
CA036994
NM_001318831.2:c.1580C>T