Canonical Allele Identifier: PA2827019826
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50125

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Glu1386Lys
CA020286
NM_001318832.2:c.4156G>A