Canonical Allele Identifier: PA916023548
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 64901

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Leu539Pro
CA015160
NM_001318832.2:c.1616T>C