Canonical Allele Identifier: PA2827020265
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49794

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Glu1502Lys
CA020888
NM_001318832.2:c.4504G>A