Canonical Allele Identifier: PA2827018589
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2747514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Leu1028Met
CA394285548
NM_001318832.2:c.3082C>A