Canonical Allele Identifier: PA2827019722
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207683

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Arg1353Gln
CA050701
NM_001318832.2:c.4058G>A